Olfactory Neuroblastoma, Esthesioneuroblastoma, Neoplasm of the Nasal Cavity
Conditions
Keywords
ONB, M7824, nasal tumor
Brief summary
Background: Olfactory neuroblastoma (ONB) is a rare cancer of the nasal cavity. At diagnosis, it is usually locally advanced. It tends to spread to the neck. Sometimes it spreads to the lungs and bones. Researchers want to find a better way to treat it. Objective: To learn if giving immunotherapy drug bintrafusp alfa can help ONB shrink or disappear. Eligibility: People aged 18 years and older diagnosed with recurrent or metastatic ONB that has not responded to standard treatment. Design: Participants will be screened with a medical history, blood and urine tests, and physical exam. Their ability to perform their normal activities will be assessed. They will have an electrocardiogram to evaluate their heart. They will have imaging scans and/or a nuclear bone scan, as needed. For some scans, they may receive a contrast dye. Some screening tests will be repeated during the study. Participants will receive bintrafusp alfa once every 2 weeks for 26 doses. They will get it intravenously over 60 minutes. They may get other medicines to prevent side effects. They will complete health questionnaires. Visits will last 4-6 hours. Participants may have optional tumor biopsies. Participants will have an end of treatment visit within 7 days after they stop taking the study drug. About 28 days after treatment ends, they will have a safety visit. They will have follow-up visits every 3 months for the first year, then every 6 months for years 2-5, and then once a year after that for the rest of their life. If their disease progresses, they may be eligible for re-treatment with the study drug
Detailed description
Background: Olfactory neuroblastoma (ONB, also known as esthesioneuroblastoma), is a rare malignant neoplasm of the nasal cavity. At diagnosis, ONB is often locally advanced. It tends to invade locally and has high rates of regional spread to the neck, and distally to the lungs and bones. The 10-year survival rate for ONB is reported at 46%. Standard of care treatment is surgical resection followed by adjuvant radiation. In advanced unresectable or metastatic cases, systemic chemotherapy is used off label, with agent selection based on published case series. Genomic profiling of ONB has not yet informed the utilization of an appropriate molecularly targeted treatment. High programmed death-ligand 1 (PD-L1) expression by immunohistochemistry was shown in ONB tumor samples, providing a rationale for immune checkpoint blockade in ONB. In addition, high expression of transforming growth factor beta (TGF-beta) ligands has been identified in ONB, implying that additional benefit may be achieved by combination of checkpoint blockade with TGF-beta inhibition. Bintrafusp alfa is a novel bifunctional fusion protein composed of a blocking monoclonal antibody against PD-L1 fused with the soluble extracellular domain of the human TGF-beta receptor II (TGF-betaRII), acting as a decoy target for TGF-beta. The safety profile of bintrafusp alfa in clinical trials to date has been shown to be manageable. Objective: To assess the objective response rate (ORR) to bintrafusp alfa in participants with recurrent/metastatic ONB, immune checkpoint-naive (CN) Eligibility: Participants must have histologically confirmed recurrent or metastatic ONB, not amenable to potentially curative local therapies. Participants should have received at least one line of systemic therapy including a platinum agent, with evidence of disease progression clinically or radiographically. Presence of \>= 1 lesion measurable by Response Evaluation Criteria in Solid Tumors, (RECIST) 1.1 criteria Age \>= 18 years, men and women Adequate organ function, and without serious comorbidity (e.g., autoimmune disease), that would preclude concurrent systemic treatment. Design: Single-institution, single-arm Phase II trial to determine overall response rate (ORR) in participants with recurrent/metastatic ONB treated with bintrafusp alfa. Participants will be treated with bintrafusp alfa 1200 mg every 2 weeks for 26 doses. The trial will initially enroll 12 checkpoint-naive (CN) participants; if responses are observed in one or more participants, the second stage will enroll another 9 CN participants to define the response rate to bintrafusp alfa, for a total of 21 CN participants. An additional cohort of checkpoint-resistant (CR) participants will be enrolled and evaluated separately. Initially 5 CR participants will be enrolled; if responses are observed in one or more participants, the second stage will enroll another 3 participants, for a total of up to 8 CR participants. Accrual for CR participants will end when the preset number of CN participants has been accrued.
Interventions
DRUGBintrafusp alfa/M7824
Participants will be treated with bintrafusp alfa 1200 mg every 2 weeks for 26 doses.
DRUGIbuprofen
400 mg or comparable non-steroidal anti-inflammatory drugs (NSAIDs) dose up to 2 hours before and 8 hours after the start of each dose for prophylaxis of flu-like symptoms.
DIAGNOSTIC_TESTPET scan
Screening
DIAGNOSTIC_TESTCT scan
Screening
PROCEDURETumor tissue biopsy
Baseline, and subsequent weeks as stipulated in the study calendar.
DIAGNOSTIC_TESTBrain MRI
Baseline
DIAGNOSTIC_TESTDotate scan
Baseline
DIAGNOSTIC_TESTPET FDG scan
Baseline
DIAGNOSTIC_TESTNuclear bone scan
Baseline
DIAGNOSTIC_TESTEKG
Baseline
Sponsors
National Cancer Institute (NCI)
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
-INCLUSION CRITERIA: 1. Histologically or cytologically confirmed recurrent or metastatic olfactory neuroblastoma (ONB) not amenable to potentially curative local therapies. Review of tissue samples by Pathology at the National Institutes of Health (NIH) is preferred. 2. Participants must have measurable disease, per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1. A previously treated lesion by radiotherapy can be chosen as the target lesion only if progression in the respective lesion has been demonstrated during or following radiotherapy. 3. Participants should have received at least one line of systemic therapy including a platinum agent, with evidence of disease progression clinically or radiographically. 4. Men or Women \>=18 years of age on day of signing informed consent. Because no dosing or adverse event data are currently available on the use of bintrafusp alfa in participants \<18 years of age, children are excluded from this study. 5. Eastern Cooperative Oncology Group (ECOG) performance status (PS) =\<2. 6. Participants must have adequate organ and marrow function as defined below: * Absolute neutrophil count (ANC) \>=1,500/mcL * Hemoglobin \>=9 g/dL (transfusions allowed) * Platelets \>=100,000/mcL * Serum Creatinine \<= 1.5 x upper limit of normal (ULN) OR Measured creatinine clearance (CrCl) or estimated glomerular filtration rate (eGFR) by Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula may be used to estimate CrCl/eGFR \>=30 mL/min/1.73m\^2 for participant with creatinine levels \> 1.5 x institutional ULN * Serum total bilirubin \<=1.5 x upper limit of normal (ULN) OR Direct bilirubin \<=ULN for participants with total bilirubin levels \>1.5 x ULN * Aspartate aminotransferase (AST) serum glutamic oxaloacetic transaminase (SGOT) and alanine aminotransferase (ALT) serum glutamic-pyruvic transaminase (SGPT) \<=2.5 x ULN 7. The effects of immunotherapy on the developing human fetus are unknown. Therefore, participants must use effective methods of contraception (such as implants, injectables, combined oral contraceptives, intrauterine device (IUDs), sexual abstinence or vasectomized partner). * Women of child-bearing potential (WOCBP: any woman who has experienced menarche and has not had hysterectomy or bilateral oophorectomy or is not postmenopausal (amenorrheic 12 months or more following cessation of exogenous hormonal treatments; if \<50 years old need follicle stimulating hormone (FSH) in the post-menopausal range)) must agree to use highly effective contraception prior to study entry and for up to 65 days following the last dose of study treatment. * Men must agree to use highly effective contraception prior to study entry and up to 125 days following the last dose of study treatment. * Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. 8. Participants with bone metastases or hypercalcemia on intravenous bisphosphonate treatment, zolendronic acid, denosumab, or similar agents are eligible to participate and may continue this treatment. 9. Participants with treated central nervous system (CNS) ONB lesions are eligible if follow-up brain imaging after at least a month following central nervous system (CNS)-directed therapy shows no evidence of progression. 10. Participants with new or progressive non-intraparenchymal CNS ONB lesions are eligible if the treating physician determines that immediate CNS specific treatment is not required and is unlikely to be required during the first cycle of therapy. 11. Human immunodeficiency virus (HIV)-positive participants must have cluster of differentiation 4 (CD4) count \>= 200 cells per cubic millimeter at enrollment, be on stable antiretroviral therapy for at least 4 weeks and have no reported opportunistic infections or Castleman's disease within 12 months prior to enrollment. 12. For participants with serological evidence of chronic hepatitis B virus (HBV) infection, the HBV deoxyribonucleic acid (DNA) viral load must be undetectable on suppressive therapy, if indicated. 13. For participants with serological evidence of hepatitis C virus (HCV) infection, the HCV ribonucleic acid (RNA) viral load must be negative to be eligible for study participation. 14. Ability of participant to understand and the willingness to sign a written informed consent document. 15. Must co-enroll in the following two studies. A separate inform consent will be obtained from participant for these studies. * 21-C-0009: A Natural History Study of Children and Adults with Olfactory Neuroblastoma, and * 18-DC-0051: Biospecimen procurement for NIDCD clinical protocols
Exclusion criteria
1. Anticancer treatment, concurrent or prior (chemotherapy, monoclonal antibody, cytokine therapy, immune therapy, targeted small molecule therapy) or any investigational drug, within 4 weeks or 5 half-lives (whichever shorter) prior to the first drug administration. All residual treatment-related toxicities must have resolved or be minimal and not constitute a safety risk. Note: Palliative radiotherapy is permitted concurrently or within the pretreatment period. Subjects receiving bisphosphonates or denosumab are eligible provided treatment was initiated at least 14 days before treatment. 2. Participants who received prior checkpoint blockade therapy and were taken off treatment for serious adverse events related to immuno-therapy are excluded. 3. Major surgery within 4 weeks prior to the first drug administration (minimally invasive procedures such as diagnostic biopsies are permitted). 4. Active or prior documented autoimmune or inflammatory diseases that might deteriorate on immunostimulatory agent (including colitis or Crohn's disease, systemic lupus erythematosus, sarcoidosis, vasculitis, Grave's disease, hypophysitis, uveitis, rheumatoid arthritis etc.), except the following: * Type I diabetes mellitus * Chronic skin conditions that do not require systemic therapy (including eczema, vitiligo, alopecia, psoriasis) * Hypothyroidism (e.g., post-Hashimoto thyroiditis) stable, on hormone replacement * Mild autoimmune disease not active in the last 5 years may be eligible after consultation with the principal investigator. 5. Current use of immunosuppressive medication within 14 days before the first dose of the study medication, except the following: * Intranasal, inhaled, topical glucocorticoids; locally injected glucocorticoids (i.e. intra-articular, intra-ocular) * Systemic glucocorticoids at physiologic doses (generally \<= 10 mg prednisone or equivalent per day) * Glucocorticoids as premedication for contrast-enhanced studies is allowed prior to enrollment and on study. 6. Uncontrolled intercurrent chronic or acute illness including, but not limited to the following, that may limit interpretation of results or increase risk to the participant in the judgment of the investigator: * Bleeding diathesis or recent (\<3 months) clinically significant bleeding event. * Prior organ transplantation including allogenic stem-cell transplantation * Impaired cardiovascular function or clinically significant cardiovascular disease, including, but not limited to, any of the following: * cerebral vascular accident/stroke (\< 3 months prior to enrollment), * acute coronary syndromes (including myocardial infarction \< 6 months prior to enrollment, unstable angina), * Congestive Heart Failure (\>= New York Heart Association Classification Class III); CHF Class II must have been stable for 3 months prior to enrollment * history or presence of clinically significant cardiac arrhythmia including resting bradycardia, uncontrolled atrial fibrillation or paroxysmal supraventricular tachycardia (controlled arrhythmias, e.g., stable atrial fibrillation, may be allowed at the discretion of the investigator), * history of myocarditis * History of idiopathic pulmonary fibrosis, drug-induced or idiopathic pneumonitis, active interstitial lung disease, blood oxygen saturation \<90% at rest (on ambient air). * Clinically significant hepatic disease. * Active infection requiring systemic therapy (minor infections may be allowed at the discretion of the investigator). 7. Subjects unwilling to accept blood products as medically indicated. 8. Vaccination with live vaccines within 4 weeks of the first dose of treatment and while on study is prohibited. Inactivated vaccines may be administered. 9. History of allergic reactions or hypersensitivity attributed to compounds of similar chemical or biologic composition to bintrafusp alfa. Participants with history of severe hypersensitivity reaction to monoclonal antibodies (grade \>= 3 National Cancer Institute (NCI)-Common Terminology Criteria for Adverse Events (CTCAE) v5) will be evaluated by the allergy/immunology team prior to enrollment. 10. History of second malignancy within 3 years of enrollment except for the following: adequately treated localized basal cell or squamous skin cancer, cervical carcinoma in situ, superficial bladder cancer, other localized malignancy which has been adequately treated or malignancy which does not require active systemic treatment (e.g., low risk chronic lymphocytic leukemia (CLL). 11. Pregnant or breastfeeding women are excluded from this study because the study medications have not been tested in pregnant women and there is potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with the study medications, breastfeeding should be discontinued if the mother is treated on this protocol.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Participants With an Objective Response Rate (ORR) According to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 | Cycle 1 (28 days) | ORR is defined as the percentage of evaluable participants who experience a response evaluated by the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 reported along with a 95% two-sided confidence interval. Complete Response (CR) is disappearance of all target lesions. Partial Response (PR) is at least a 30% decrease in the sum of the diameters of target lesions. Progressive Disease (PD) is at least a 20% increase in the sum of the diameters of target lesions. Stable Disease (SD) is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | up to 2 years | The number of participants who experience toxicity, by grade and type of toxicity related to Bintrafusp alfa (M7824) was assessed by the Common Terminology Criteria for Adverse Events (CTCAE) v5.0. Grade 1 is mild. Grade 2 is moderate. Grade 3 is severe. Grade 4 is life-threatening. Grade 5 is death related to adverse event. A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned. |
| Overall Survival (OS) | Through study completion, an average of 2 years | OS is defined as the time from the date of first treatment to the date of death (any cause) using the Kaplan-Meier method. |
| Duration of Response (DOR) | Through treatment completion, an average of 1 year | DOR is defined as the time measurement for complete response (CR) or partial response (PR) (whichever is first recorded) until the first documented date of progressive disease (PD) or death. ORR was evaluated by the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 using the Kaplan-Meier method and reported along with a 95% two-sided confidence interval. Complete Response (CR) is disappearance of all target lesions. Partial Response (PR) is at least a 30% decrease in the sum of the diameters of target lesions. Progressive Disease (PD) is at least a 20% increase in the sum of the diameters of target lesions. |
| Progression Free Survival (PFS) | Through treatment completion, an average of 1 year | PFS is defined as the time from the date of first treatment to the date of disease progression or death (any cause) whichever occurs first, using the Kaplan-Meier method and reported along with a 95% confidence interval. Disease progression was evaluated by the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 and is at least a 20% increase in the sum of the diameters of target lesions. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0) | Adverse Events were monitored/assessed from first drug administration through 30 days after the last dose of study drug is administered, an average of 6 months. | Here is the number of participants with serious and/or non-serious adverse events assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa-Immune Checkpoint Treatment with Bintrafusp alfa
Bintrafusp alfa/M7824: Participants will be treated with bintrafusp alfa 1200 mg intravenous over 60 minutes (+/- 20 minutes) once every 2 weeks for 26 doses. | 9 |
| Cohort 2/Arm 1: Treatment With Bintrafusp Alfa- Immune Checkpoint Blockade Resistant (ICB-R) Treatment with Bintrafusp alfa
Bintrafusp alfa/M7824: Participants will be treated with bintrafusp alfa 1200 mg intravenous over 60 minutes (+/- 20 minutes) once every 2 weeks for 26 doses. | 2 |
| Total | 11 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Adverse Event | 1 | 0 |
| Overall Study | Discontinuation per protocol | 1 | 0 |
| Overall Study | Disease progression | 5 | 2 |
| Overall Study | Withdrawal by Subject | 1 | 0 |
Baseline characteristics
| Characteristic | Cohort 1/Arm 1: Treatment With Bintrafusp Alfa-Immune Checkpoint | Cohort 2/Arm 1: Treatment With Bintrafusp Alfa- Immune Checkpoint Blockade Resistant (ICB-R) | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 2 Participants | 0 Participants | 2 Participants |
| Age, Categorical Between 18 and 65 years | 7 Participants | 2 Participants | 9 Participants |
| Age, Continuous | 59.11 years STANDARD_DEVIATION 7.57 | 53 years STANDARD_DEVIATION 2.83 | 58 years STANDARD_DEVIATION 7.27 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 3 Participants | 0 Participants | 3 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 6 Participants | 2 Participants | 8 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 9 Participants | 2 Participants | 11 Participants |
| Region of Enrollment United States | 9 participants | 2 participants | 11 participants |
| Sex: Female, Male Female | 2 Participants | 1 Participants | 3 Participants |
| Sex: Female, Male Male | 7 Participants | 1 Participants | 8 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 1 / 9 | 1 / 2 |
| other Total, other adverse events | 9 / 9 | 2 / 2 |
| serious Total, serious adverse events | 3 / 9 | 2 / 2 |
Outcome results
Primary
Percentage of Participants With an Objective Response Rate (ORR) According to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1
ORR is defined as the percentage of evaluable participants who experience a response evaluated by the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 reported along with a 95% two-sided confidence interval. Complete Response (CR) is disappearance of all target lesions. Partial Response (PR) is at least a 30% decrease in the sum of the diameters of target lesions. Progressive Disease (PD) is at least a 20% increase in the sum of the diameters of target lesions. Stable Disease (SD) is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD.
Time frame: Cycle 1 (28 days)
Population: Only the immune checkpoint-naïve participants will be included in the primary endpoint analysis as pre-specified by the protocol. 8/9 participants were analyzed because one participant was non-evaluable for response
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Percentage of Participants With an Objective Response Rate (ORR) According to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 | Complete Response | 0 Percentage of participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Percentage of Participants With an Objective Response Rate (ORR) According to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 | Partial Response | 0 Percentage of participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Percentage of Participants With an Objective Response Rate (ORR) According to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 | Stable Disease | 37.5 Percentage of participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Percentage of Participants With an Objective Response Rate (ORR) According to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 | Progressive Disease | 62.5 Percentage of participants |
Secondary
Duration of Response (DOR)
DOR is defined as the time measurement for complete response (CR) or partial response (PR) (whichever is first recorded) until the first documented date of progressive disease (PD) or death. ORR was evaluated by the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 using the Kaplan-Meier method and reported along with a 95% two-sided confidence interval. Complete Response (CR) is disappearance of all target lesions. Partial Response (PR) is at least a 30% decrease in the sum of the diameters of target lesions. Progressive Disease (PD) is at least a 20% increase in the sum of the diameters of target lesions.
Time frame: Through treatment completion, an average of 1 year
Population: No participants experienced Complete or Partial Response therefore Duration of Response could not be assessed.
Secondary
Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity
The number of participants who experience toxicity, by grade and type of toxicity related to Bintrafusp alfa (M7824) was assessed by the Common Terminology Criteria for Adverse Events (CTCAE) v5.0. Grade 1 is mild. Grade 2 is moderate. Grade 3 is severe. Grade 4 is life-threatening. Grade 5 is death related to adverse event. A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned.
Time frame: up to 2 years
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 2 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 2 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 3 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 2 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 1 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 0 Participants |
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 3 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 2 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 3 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 3 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 1 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Participants in Cohort 1/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 1 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 2 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 3 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 1 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 4 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Folliculitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Esophageal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Constipation | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Diarrhea | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pharyngeal mucositis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Insomnia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Cardiac troponin I increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Atrioventricular block first degree | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Flu like symptoms | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Dry eye | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Platelet count decreased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Anemia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Serious: Metabolism and nutrition disorders: Immune-mediated diabetes | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Epistaxis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hypothyroidism | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pneumonitis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Pruritus | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Lipase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Bruising | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hemorrhoidal hemorrhage | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Arthralgia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Electrocardiogram T wave abnormal | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Rash maculo-papular | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Neoplasms benign, malignant and unspecified: Keratoacanthoma | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Acute kidney injury | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Hyperhidrosis | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Aspartate aminotransferase increased | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Headache | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Oral dysesthesia | 0 Participants |
| Participants in Cohort 2/Arm 1 With Grade 5 Toxicity | Number of Participants Who Experience a Toxicity Related to Bintrafusp Alfa (M7824), by Grades (1, 2, 3, 4 and/or 5) and Type of Toxicity | Non-serious: Skin hypopigmentation: Vitiligo | 0 Participants |
Secondary
Overall Survival (OS)
OS is defined as the time from the date of first treatment to the date of death (any cause) using the Kaplan-Meier method.
Time frame: Through study completion, an average of 2 years
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Overall Survival (OS) | NA Months |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Overall Survival (OS) | 2.1 Months |
Secondary
Progression Free Survival (PFS)
PFS is defined as the time from the date of first treatment to the date of disease progression or death (any cause) whichever occurs first, using the Kaplan-Meier method and reported along with a 95% confidence interval. Disease progression was evaluated by the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 and is at least a 20% increase in the sum of the diameters of target lesions.
Time frame: Through treatment completion, an average of 1 year
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Progression Free Survival (PFS) | 9.3 Months |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Progression Free Survival (PFS) | 2.99 Months |
Other Pre-specified
Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0)
Here is the number of participants with serious and/or non-serious adverse events assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned.
Time frame: Adverse Events were monitored/assessed from first drug administration through 30 days after the last dose of study drug is administered, an average of 6 months.
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Cohort 1/Arm 1: Treatment With Bintrafusp Alfa - Immune Checkpoint | Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0) | 9 Participants |
| Participants in Cohort 1/Arm 1 With Grade 2 Toxicity | Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v5.0) | 2 Participants |