Non-small Cell Lung Carcinoma, Solid Tumors
Conditions
Keywords
Heat shock protein 90, Advanced solid tumors, Non-small cell lung carcinoma, Epidermal growth factor receptor, Tyrosine kinase inhibitor acquired resistance, Non-small cell lung carcinoma with acquired resistance to erlotinib, gefitinib, afatinib or others.
Brief summary
This phase 1 clinical trial is intended to understand the safety and tolerability of a new anticancer drug in subjects with advanced solid tumors. The patients who qualify for the study will receive a once daily dose of the drug taken by mouth and will undergo several tests to measure the drug in the blood and to understand the safety, tolerability and any effect of the drug on the tumor. The antitumor effect of the drug is not known in human.
Detailed description
The study will be conducted in two parts. Part 1 is a dose escalation study in which subjects in each cohort will be given increasing doses of the study drug until a maximum tolerated dose (MTD) or maximum administered dose (MAD) is determined as the recommended phase 2 dose (RP2D). The drug will be administered as oral capsules once daily in 21 day cycles, with no interruption between cycles if no unacceptable treatment-related toxicity or tumor progression are observed. After determining the RP2D, Part 2 of the study, which is a dose expansion study will begin in which subjects with advanced non-small cell lung cancer who developed acquired resistance to epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKI), erlotinib, gefitinib, afatinib (and others) or whose tumors carry an ALK translocation and are resistant to ALK inhibitor therapy, will be treated with DS-2248 at RP2D. The drug will be administered as oral capsules once daily in 21 day cycles, with no interruption between cycles if no unacceptable treatment-related toxicity or tumor progression are observed.
Interventions
DRUGDS-2248
Oral capsules, of various strengths (1, 5 , 20 ,or 50 milligrams), once daily during 21-day cycles, until unacceptable treatment-related toxicity or tumor progression are observed.
Sponsors
Daiichi Sankyo UK Ltd.
Daiichi Sankyo
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. A pathologically documented advanced solid malignant tumor refractory to standard treatment or for which no standard treatment is available. 2. Eastern Cooperative Oncology Group (ECOG) performance status ≤1. 3. Have adequate bone marrow function, defined as: * Platelet count ≥100x10\^9/L or more. * Hemoglobin (Hb) level ≥9.0 g/dL. * Absolute neutrophil count ≥1.5 x 10\^9/L. 4. Have adequate renal function, defined as: \- Creatinine clearance ≥60 mL/min, as calculated using the modified Cockcroft-Gault equation AND creatinine ≤1.5 times upper limit of normal(ULN). 5. Have adequate hepatic function, defined as: * Aspartate aminotransferase (AST) levels ≤3 times ULN (if liver metastases are present, ≤5x ULN) * Alanine aminotransferase (ALT) levels ≤3x ULN (if liver metastases are present, ≤5x ULN * Bilirubin ≤1.5x ULN 6. Have adequate blood clotting function, defined as: \- Prothrombin time and activated partial thromboplastin time ≤1.5x ULN 7. Participants should be able to provide written informed consent, comply with protocol visits and procedures, be able to take oral medication, and not have any active infection or chronic co-morbidity that would interfere with therapy. 8. Participants (male and female) of childbearing/reproductive potential must agree to use double-barrier contraceptive measures or avoid intercourse during the study and for 90 days after the last dose of study drug. If female and of childbearing potential, must have a negative result of a pregnancy test (serum or urine)within 72 hours prior to initiating study treatment. Surgically sterile individuals and postmenopausal females are considered not having child-bearing potential. 9. Participants must be fully informed about their illness and the investigational nature of the study protocol (including foreseeable risks and possible side effects) and must sign and date an Institutional Review Board approved informed consent form (including Health Insurance Portability and Accountability Act authorization, if applicable) before performance of any study-specific procedures or tests. 10. Participants must be willing to provide pre-existing diagnostic or resected tumor samples, such as formalin-fixed paraffin-embedded sections, if available. Providing fresh pre-treatment tumor biopsy is optional for participants in dose escalation cohorts and in dose expansion Stage 1. Post-treatment biopsies are optional for all the participants in the study (dose escalation and dose expansion cohorts). Additional Inclusion Criteria for Part 2 (Dose Expansion) 1. Pathologically documented stage IIIB/IV non-small cell lung cancer. 2. Measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST) criteria, Version 1.1. 3. Participants must meet 1 of the following 3 criteria in order to be included in Part 2: 1. Acquired resistance to reversible Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor (EGFR-TKI), which should meet the following criteria: * Previous treatment with single-agent therapy (erlotinib, gefitinib, afatinib or others). * Either of the following: A tumor that harbors an EGFR mutation known to be associated with drug sensitivity (i.e., G719X, exon 19 deletion, L858R, L861Q) -OR- Prior objective clinical benefit from EGFR-TKI, as evidenced by complete response (CR), partial response (PR), or stable disease (SD) ≥6 months as defined by RECIST or World Health Organization criteria. * Systemic progression of disease as defined by RECIST or World Health Organization criteria while treatment with gefitinib, erlotinib, afatinib or others. * No intervening therapy other than EGFR-TKIs (erlotinib, gefitinib, afatinib or others) after progression on an EGFR-TKI. * Pre-treatment biopsy (performed via bronchoscopy or imaging guidance) for molecular testing of the tumor is desired but not mandatory for enrollment in Stage 1. However, pre-treatment biopsy within 21 days prior to the first day of treatment is required for enrollment in Stage 2. 2. Presence of ALK fusion gene in the tumor demonstrated by fluorescence in situ hybridization (FISH) and the participant has acquired resistance to ALK inhibitor therapy.
Exclusion criteria
1. History of second malignancies or primary central nervous system malignancies, except adequately treated non-melanoma skin cancer, curatively treated in-situ disease, or other solid tumors curatively treated, with no evidence of disease for ≥3 years. 2. Gastrointestinal diseases that could affect the absorption of DS-2248. 3. Subjects with peptic ulcer disease requiring on-going treatment with pH-modifiers 4. Subjects with history of inflammatory bowel disease. 5. Subjects with retinal or uveal diseases including macular degeneration with central vision loss, retinal detachment, diabetic retinopathy, and uveitis. 6. Recipient of a stem cell or bone marrow transplant. 7. Has a concomitant medical condition that would increase the risk of toxicity, in the opinion of the Investigator or Sponsor. 8. Clinically active brain metastases, defined as untreated and symptomatic, or requiring therapy with steroids or anticonvulsants to control associated symptoms. Subjects with treated brain metastases that are no longer symptomatic and who require no treatment with steroids may be included in the study if they have recovered from the acute toxic effect of radiotherapy. A minimum of 4 weeks must have elapsed between the end of whole brain radiotherapy and study enrollment (2 weeks for stereotactic radiotherapy). 9. Has unresolved toxicities from previous anti-cancer therapy, defined as toxicities (other than alopecia) not yet resolved to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), Version 4.0, Grade ≤1 or baseline. Subjects with chronic Grade 2 toxicities may be eligible per the discretion of the Investigator or Sponsor (e.g., Grade 2 chemotherapy-induced neuropathy). 10. Systemic treatment with anticancer therapy, antibody-based therapy, retinoid therapy, or hormonal therapy (except megestrol acetate as supportive care) within 3 weeks before study drug treatment; or treatment with nitrosoureas or mitomycin C within 6 weeks before study drug treatment; or treatment with small-molecule Tyrosine Kinase Inhibitors within 7 days for erlotinib and afatinib and 10 days for gefitinib before study drug treatment. Previous and concurrent use of hormone replacement therapy, the use of gonadotropin-releasing hormone modulators for prostate cancer, and the use of somatostatin analogs for neuroendocrine tumors are permitted. 11. Therapeutic radiation therapy or major surgery within 4 weeks before study drug treatment or palliative radiation therapy within 2 weeks before study drug treatment. 12. Participation in a clinical drug study within 3 weeks for small-molecule TKIs before study drug treatment, or current participation in other investigational procedures. 13. Concomitant treatment with potent inducers or potent inhibitors of cytochrome P450 3A4 (CYP3A4). 14. Concomitant treatment with a medication known to cause renal tubular damage or reduce renal perfusion at the dose administered, including aminoglycosides, amphotericin B, pentamidine, nonsteroidal anti-inflammatory drugs, and zoledronate. 15. Corrected QT interval (QTc by Bazett's formula) prolongation at rest, where the mean QTc interval is \>450 msec based on triplicate ECG. 16. Pregnant or breastfeeding. 17. Substance abuse or medical, psychological, or social conditions that may, in the opinion of the Investigator, interfere with the subject's participation in the clinical study or evaluation of the clinical study results. 18. Less than 1 week since using systemically acting drugs that increase gastric pH, such as H2-blockers and proton pump inhibitors. Antacids should be avoided within 48 hours of the first dose of DS-2248. 19. Use of St. John's Wort (hypericin) is not permitted for 30 days before and during the study. Foods or beverages containing grapefruit should be avoided within 48 hours before and during the study. Additional
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months | Objective response rate was defined as the sum of complete response (CR) and partial response (PR) rates. CR was defined as a disappearance of all target lesions; any pathological lymph nodes (whether target or non-target) must have had a reduction in short axis to \<10 mm. PR was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months | Disease control rate (DCR) was defined as the sum of complete response (CR) and partial response (PR) rates, and stable disease (SD) rate for a minimum of 12 weeks. Complete response (CR) was defined as a disappearance of all target lesions; any pathological lymph nodes (whether target or non-target) must have had a reduction in short axis to \<10 mm. Partial response (PR) was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. Stable disease (SD) was defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease (at least a 20% increase in the sum of diameters of target lesions), taking as reference the smallest sum diameters while on study. |
| Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months | Duration of response measured from the time at which criteria were first met for complete (CR) or partial response (PR) until the first date that progressive disease (PD) was objectively documented. Participants who had not progressed at the data cut-off date were censored at their last evaluable tumor assessment date. Duration of stable disease (SD) measured from the date of enrollment until the first date that criteria for disease progression were met. The minimum time interval for the duration of SD was 6 weeks. Participants who had not progressed at the data cut-off date were censored at their last evaluable tumor assessment date. |
| Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months | Progression-free survival (PFS) defined as the time from the date of enrollment to the earlier of the dates of the first objective documentation of radiographic disease progression (as per RECIST V1.1) or death due to any cause. Participants who were alive with no objective documentation of (radiographic) disease progression by the data cut-off date were censored at the date of their last evaluable tumor assessment. Participants who were lost to follow-up or withdrew early from the study with no documented disease progression were censored at the last evaluable tumor assessment. |
| Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15 | — |
| Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months | Complete response (CR) was defined as a disappearance of all target lesions; any pathological lymph nodes (whether target or non-target) must have had a reduction in short axis to \<10 mm. Partial response (PR) was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. Progressive disease (PD) was defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this included the baseline sum if that was the smallest on study). In addition to the relative increase of 20%, the sum must also have demonstrated an absolute increase of at least 5 mm. Stable disease (SD) was defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum diameters while on study. Objective response rate (ORR) was defined as the sum of CR and PR rates. |
| Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15 | — |
| Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15 | — |
| Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15 | — |
| Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Baseline up to 30 days post last dose, up to 2 years 11 months | A treatment-emergent adverse event (TEAE) is defined as an adverse event that emerges during treatment, having been absent at pre-treatment; or reemerges during treatment, having been present at baseline but stopped prior to treatment; or worsens in severity after starting treatment relative to the pre-treatment state, when the AE is continuous. A DS-2248-related TEAE is an TEAE that is related to DS-2248 in the relationship. |
| Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15 | — |
Countries
United States
Participant flow
Recruitment details
A total of 60 participants who met all inclusion and no exclusion criteria were enrolled in the study.
Pre-assignment details
Part 1: Dose escalation began with an accelerated titration design, with a starting dose of DS-2248 0.6 mg/m\^2 once daily. Part 2: Dose expansion was assessed in participants with Stage IIIB/IV non-small cell lung cancer with resistance to epidermal growth factor receptor tyrosine kinase inhibitor or ALK inhibitor therapy.
Participants by arm
| Arm | Count |
|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 Participants who received oral DS-2248 0.6 mg/m\^2 once daily. | 2 |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 Participants who received oral DS-2248 1.2 mg/m\^2 once daily. | 3 |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 Participants who received oral DS-2248 1.8 mg/m\^2 once daily. | 5 |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 Participants who received oral DS-2248 2.7 mg/m\^2 once daily. | 7 |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 Participants who received oral DS-2248 3.5 mg/m\^2 once daily. | 3 |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 Participants who received oral DS-2248 4.5 mg/m\^2 once daily. | 6 |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 Participants who received oral DS-2248 5.85 mg/m\^2 once daily. | 7 |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 Participants who were epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI)-resistant and received oral 4.5 mg/m\^2 once daily. | 12 |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 Participants who were ALK-inhibitor resistant and received oral 4.5 mg/m\^2 once daily. | 12 |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 Participants who were ALK treatment naive and received oral 4.5 mg/m\^2 once daily. | 3 |
| Total | 60 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 | FG003 | FG004 | FG005 | FG006 | FG007 | FG008 | FG009 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Part 1 | Adverse Event | 0 | 0 | 3 | 1 | 0 | 0 | 2 | 0 | 0 | 0 |
| Part 1 | Clinical disease progression | 0 | 0 | 1 | 0 | 0 | 2 | 2 | 0 | 0 | 0 |
| Part 1 | Death due to disease progression | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 |
| Part 1 | Other | 0 | 2 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 |
| Part 1 | Progressive disease | 2 | 1 | 1 | 6 | 2 | 4 | 2 | 0 | 0 | 0 |
| Part 2 | Adverse Event | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 0 |
| Part 2 | Clinical disease progression | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 2 | 0 | 0 |
| Part 2 | Other | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
| Part 2 | Progressive disease | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 8 | 7 | 2 |
| Part 2 | Withdrawal by Subject | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 4 | 0 |
Baseline characteristics
| Characteristic | Total | Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Part 2, ALK-naive: DS-2248 4.5 mg/m^2 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 20 Participants | 2 Participants | 1 Participants | 2 Participants | 1 Participants | 0 Participants | 3 Participants | 5 Participants | 4 Participants | 2 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 40 Participants | 3 Participants | 2 Participants | 5 Participants | 2 Participants | 6 Participants | 4 Participants | 7 Participants | 8 Participants | 0 Participants | 3 Participants |
| Age, Continuous | 58.8 years STANDARD_DEVIATION 12.9 | 61.0 years STANDARD_DEVIATION 10.8 | 58.7 years STANDARD_DEVIATION 16.6 | 60.1 years STANDARD_DEVIATION 11.9 | 53.0 years STANDARD_DEVIATION 17.4 | 49.8 years STANDARD_DEVIATION 11.6 | 61.4 years STANDARD_DEVIATION 12.9 | 58.8 years STANDARD_DEVIATION 11.2 | 59.8 years STANDARD_DEVIATION 11.8 | 75.0 years STANDARD_DEVIATION 0 | 51.7 years STANDARD_DEVIATION 2.5 |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 7 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 1 Participants | 0 Participants | 3 Participants | 3 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 3 Participants | 0 Participants | 1 Participants | 0 Participants | 0 Participants | 0 Participants | 1 Participants | 0 Participants | 1 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 50 Participants | 5 Participants | 2 Participants | 7 Participants | 3 Participants | 5 Participants | 6 Participants | 9 Participants | 8 Participants | 2 Participants | 3 Participants |
| Region of Enrollment United States | 60 participants | 5 participants | 3 participants | 7 participants | 3 participants | 6 participants | 7 participants | 12 participants | 12 participants | 2 participants | 3 participants |
| Sex: Female, Male Female | 29 Participants | 4 Participants | 2 Participants | 4 Participants | 1 Participants | 2 Participants | 2 Participants | 6 Participants | 5 Participants | 1 Participants | 2 Participants |
| Sex: Female, Male Male | 31 Participants | 1 Participants | 1 Participants | 3 Participants | 2 Participants | 4 Participants | 5 Participants | 6 Participants | 7 Participants | 1 Participants | 1 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk | EG004 affected / at risk | EG005 affected / at risk | EG006 affected / at risk | EG007 affected / at risk | EG008 affected / at risk | EG009 affected / at risk |
|---|---|---|---|---|---|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 2 | 0 / 3 | 0 / 5 | 0 / 7 | 1 / 3 | 0 / 6 | 0 / 7 | 0 / 12 | 0 / 12 | 0 / 3 |
| other Total, other adverse events | 2 / 2 | 3 / 3 | 5 / 5 | 7 / 7 | 3 / 3 | 6 / 6 | 7 / 7 | 12 / 12 | 10 / 12 | 3 / 3 |
| serious Total, serious adverse events | 0 / 2 | 1 / 3 | 2 / 5 | 3 / 7 | 1 / 3 | 1 / 6 | 1 / 7 | 1 / 12 | 0 / 12 | 0 / 3 |
Outcome results
Primary
Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Objective response rate was defined as the sum of complete response (CR) and partial response (PR) rates. CR was defined as a disappearance of all target lesions; any pathological lymph nodes (whether target or non-target) must have had a reduction in short axis to \<10 mm. PR was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters.
Time frame: Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months
Population: Objective response rate was assessed in the Full Analysis Set.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Objective Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
Secondary
Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Duration of response measured from the time at which criteria were first met for complete (CR) or partial response (PR) until the first date that progressive disease (PD) was objectively documented. Participants who had not progressed at the data cut-off date were censored at their last evaluable tumor assessment date. Duration of stable disease (SD) measured from the date of enrollment until the first date that criteria for disease progression were met. The minimum time interval for the duration of SD was 6 weeks. Participants who had not progressed at the data cut-off date were censored at their last evaluable tumor assessment date.
Time frame: Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months
Population: Duration of stable disease was assessed in participants in which data were available in the Full Analysis Set.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 15.00 weeks |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 7.9 weeks |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 13.29 weeks |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 9.50 weeks |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 6.64 weeks |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 12.86 weeks |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 10.57 weeks |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Duration of Stable Disease Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 13.1 weeks |
Secondary
Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Complete response (CR) was defined as a disappearance of all target lesions; any pathological lymph nodes (whether target or non-target) must have had a reduction in short axis to \<10 mm. Partial response (PR) was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. Progressive disease (PD) was defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this included the baseline sum if that was the smallest on study). In addition to the relative increase of 20%, the sum must also have demonstrated an absolute increase of at least 5 mm. Stable disease (SD) was defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, taking as reference the smallest sum diameters while on study. Objective response rate (ORR) was defined as the sum of CR and PR rates.
Time frame: Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months
Population: Best overall response was assessed in the Full Analysis Set.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 1 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 1 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 1 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 1 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 3 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 5 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 2 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 2 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 3 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 2 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 4 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 6 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 2 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 7 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Progressive disease | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed CR | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Non-evaluable | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Confirmed PR | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Best Overall Response Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Stable disease | 1 Participants |
Secondary
Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Disease control rate (DCR) was defined as the sum of complete response (CR) and partial response (PR) rates, and stable disease (SD) rate for a minimum of 12 weeks. Complete response (CR) was defined as a disappearance of all target lesions; any pathological lymph nodes (whether target or non-target) must have had a reduction in short axis to \<10 mm. Partial response (PR) was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. Stable disease (SD) was defined as neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progressive disease (at least a 20% increase in the sum of diameters of target lesions), taking as reference the smallest sum diameters while on study.
Time frame: Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months
Population: Disease control rate was assessed in the Full Analysis Set.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 2 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 2 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Disease Control Rate Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1 Participants |
Secondary
Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
A treatment-emergent adverse event (TEAE) is defined as an adverse event that emerges during treatment, having been absent at pre-treatment; or reemerges during treatment, having been present at baseline but stopped prior to treatment; or worsens in severity after starting treatment relative to the pre-treatment state, when the AE is continuous. A DS-2248-related TEAE is an TEAE that is related to DS-2248 in the relationship.
Time frame: Baseline up to 30 days post last dose, up to 2 years 11 months
Population: Treatment-emergent adverse events were assessed in the Safety Analysis Set.
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 1 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 1 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 1 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 3 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 3 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 4 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 1 Participants |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 2 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 5 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 3 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 1 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 1 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 1 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 1 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 1 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 1 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 1 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 1 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 1 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 2 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 2 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 4 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 2 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 2 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 1 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 2 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 2 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 6 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 3 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 2 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 4 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 4 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 1 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 3 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 5 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 9 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 9 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 3 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 21 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 8 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 4 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 2 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 1 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 8 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 8 Participants |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 2 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 3 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 7 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 3 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 3 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 2 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 3 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 3 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 2 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 3 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 3 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 1 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 3 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 3 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 3 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 3 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 5 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 4 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 6 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 9 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 2 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 0 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 1 Participants |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal failure acute | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Irritability | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nystagmus | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Oedema peripheral | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Respiratory, Thoracic, and Mediastinal Disorders | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood uric acid increased | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dysgeusia | 5 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Investigations | 7 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Thrombocytopenia | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Muscular weakness | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dehydration | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Paraesthesia oral | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dizziness | 3 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Aspartate aminotransferase increased | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Reproductive System and Breast Disorders | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal pain | 2 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypoalbuminaemia | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vomiting | 2 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Skin and Subcutaneous Tissue Disorders | 4 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nausea | 4 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Flatulence | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Headache | 3 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Eye Disorders | 5 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Arthralgia | 2 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal and Connective Tissue Disorders | 3 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Photopsia | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry skin | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperphosphataemia | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Pruritus | 2 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Onychoclasis | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anaemia | 4 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypokalaemia | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Anorectal discomfort | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Myalgia | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrointestinal Disorders | 9 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight decreased | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Musculoskeletal pain | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Immune System Disorders | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood creatinine increased | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Renal and Urinary Disorders | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Restless legs syndrome | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Nervous System Disorders | 9 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Tachycardia | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Breast tenderness | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperuricaemia | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperglycaemia | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Decreased appetite | 3 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Metabolism and Nutrition Disorders | 6 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Weight increased | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Cardiac Disorders | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hyperhidrosis | 2 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood phosphorus increased | 2 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood urea increased | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood alkaline phosphatase increased | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Alanine aminotransferase increase | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Hypersensitivity | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Fatigue | 6 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | General Disorders & Administration Site Conditions | 7 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Gastrooesophageal reflux disease | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspepsia | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Lymphopenia | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Drug-related TEAEs | 18 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Diarrhoea | 4 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Constipation | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Abdominal distension | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vitreous floaters | 2 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Vision blurred | 1 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Blood and Lymphatic Disorders | 4 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dry eye | 2 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Retinal haemorrhage | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Proteinuria | 0 Participants |
| Total - Part 2 | Summary of Drug Related Treatment Emergent Adverse Events Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | Dyspnoea | 0 Participants |
Secondary
Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Time frame: Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15
Population: Pharmacokinetic parameters were assessed in the Pharmacokinetic Analysis Set for which data were available.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 76.47 ng*h/mL | — |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 122.56 ng*h/mL | Standard Deviation 60.78 |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 186.16 ng*h/mL | Standard Deviation 102.2 |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 362.31 ng*h/mL | — |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 356.01 ng*h/mL | — |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 675.57 ng*h/mL | Standard Deviation 478.25 |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 837.50 ng*h/mL | Standard Deviation 606.7 |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 501.21 ng*h/mL | Standard Deviation 161.8 |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 645.62 ng*h/mL | Standard Deviation 257.3 |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Area Under the Concentration Versus Time Curve From Zero to Infinity Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 459.96 ng*h/mL | — |
Secondary
Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Time frame: Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15
Population: Pharmacokinetic parameters were assessed in the Pharmacokinetic Analysis Set for which data were available.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 6.46 ng/mL | Standard Deviation 1.54 |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 14.69 ng/mL | Standard Deviation 7.37 |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 25.60 ng/mL | Standard Deviation 9.62 |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 63.27 ng/mL | Standard Deviation 31.02 |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 71.30 ng/mL | Standard Deviation 37.99 |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 77.15 ng/mL | Standard Deviation 32.17 |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 126.61 ng/mL | Standard Deviation 67.6 |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 82.56 ng/mL | Standard Deviation 34.22 |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 81.45 ng/mL | Standard Deviation 53.71 |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 84.97 ng/mL | Standard Deviation 34.16 |
Secondary
Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Time frame: Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15
Population: Pharmacokinetic parameters were assessed in the Pharmacokinetic Analysis Set for which data were available.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 9.58 hours | — |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 7.81 hours | Standard Deviation 1.75 |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 8.11 hours | Standard Deviation 1.79 |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 10.78 hours | — |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 8.57 hours | — |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 8.62 hours | Standard Deviation 1.21 |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 10.05 hours | Standard Deviation 0.73 |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 9.94 hours | Standard Deviation 0.93 |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 9.23 hours | Standard Deviation 0.55 |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Terminal Half-life Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 6.76 hours | — |
Secondary
Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Time frame: Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15
Population: Pharmacokinetic parameters were assessed in the Pharmacokinetic Analysis Set for which data were available.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 2.0 hours | Standard Deviation 1.4 |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1.7 hours | Standard Deviation 0.6 |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1.1 hours | Standard Deviation 0.6 |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1.5 hours | Standard Deviation 0.9 |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1.2 hours | Standard Deviation 0.8 |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 2.3 hours | Standard Deviation 1 |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 2.1 hours | Standard Deviation 0.7 |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1.8 hours | Standard Deviation 0.9 |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 1.6 hours | Standard Deviation 0.9 |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Time at Maximum Concentration Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 2.0 hours | Standard Deviation 1.1 |
Secondary
Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Time frame: Cycle 1, Day 1 predose, 0.5, 1, 2, 3, 4, 6, and 8 h postdose; Cycle 1, Day 2 and Day 15; Cycle 1, Day 8 predose, 1 and 6 h postdose; Cycle 2 and 3, Day 1, 8, and 15
Population: Pharmacokinetic parameters were assessed in the Pharmacokinetic Analysis Set for which data were available.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.01 L/h | — |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.02 L/h | Standard Deviation 0.01 |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.01 L/h | Standard Deviation 0 |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.01 L/h | — |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.01 L/h | — |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.02 L/h | Standard Deviation 0.01 |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.02 L/h | Standard Deviation 0.01 |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.02 L/h | Standard Deviation 0 |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.01 L/h | Standard Deviation 0 |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Pharmacokinetic Parameter Total Body Clearance Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 0.02 L/h | — |
Secondary
Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors
Progression-free survival (PFS) defined as the time from the date of enrollment to the earlier of the dates of the first objective documentation of radiographic disease progression (as per RECIST V1.1) or death due to any cause. Participants who were alive with no objective documentation of (radiographic) disease progression by the data cut-off date were censored at the date of their last evaluable tumor assessment. Participants who were lost to follow-up or withdrew early from the study with no documented disease progression were censored at the last evaluable tumor assessment.
Time frame: Baseline up to disease progression, discontinuation of study, or death, up to 2 years 11 months
Population: Progression-free survival was assessed in the Full Analysis Set.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Part 1, Cohort 1: DS-2248 0.6 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 10.93 weeks |
| Part 1, Cohort 2: DS-2248 1.2 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 5.71 weeks |
| Part 1, Cohort 3: DS-2248 1.8 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 13.29 weeks |
| Part 1, Cohort 4: DS-2248 2.7 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 7.00 weeks |
| Part 1, Cohort 5: DS-2248 3.5 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 5.64 weeks |
| Part 1, Cohort 6: DS-2248 4.5 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 6.00 weeks |
| Part 1, Cohort 7: DS-2248 5.85 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 6.57 weeks |
| Part 2, EGFR TKI-resistant: DS-2248 4.5 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 7.21 weeks |
| Part 2, ALK-resistant: DS-2248 4.5 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 7.14 weeks |
| Part 2, ALK-naive: DS-2248 4.5 mg/m^2 | Summary of Progression-free Survival Following Oral Administration of DS-2248 in Participants With Advanced Solid Tumors | 10.00 weeks |