Carcinoma, Non-Small-Cell Lung, Endometrial Neoplasms, Neoplasm Metastasis, Small Cell Lung Carcinoma, Triple Negative Breast Cancer
Conditions
Brief summary
The purpose of this study is to measure the safety and efficacy of LY4175408 in participants with selected advanced cancer. In addition, this study will evaluate how much LY4175408 gets into the bloodstream, how it is broken down, and how long it takes the body to get rid of it. Participation could last up to 4 years.
Interventions
DRUGLY4175408
IV infusion
DRUGPembrolizumab
IV infusion
DRUGCarboplatin
IV infusion
DRUGCisplatin
IV infusion
Sponsors
Eli Lilly and Company
Study design
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Have one of the following advanced or metastatic solid tumor cancers: * Non-small cell lung cancer (NSCLC) * Small cell lung cancer (SCLC) * Endometrial cancer * Triple negative breast cancer (TNBC) (characterized by HR-negative disease and HER2-negative expression according to American Society of Clinical Oncology (ASCO) - College of American Pathologists guidelines). * Received all standard therapies for which the individual was deemed to be an appropriate candidate by the treating investigator (except in Cohort B1 and B2 expansion, which require participants who are treatment naive in the advanced metastatic setting); OR the individual is refusing the remaining most appropriate standard of care treatment; OR there is no standard therapy available for the disease. * Eastern Cooperative Oncology Group (ECOG) performance status of greater than or equal to (≤) 1. * For dose optimization/dose and expansion cohorts (Cohort A2, Cohort B/C): Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. * Cohorts B1/B2: NSCLC with no known actionable genomic alterations. ≤2 prior lines of systemic therapy for advanced or metastatic disease in safety lead-in; no prior systemic therapy in expansion
Exclusion criteria
* Prior treatment with a protein tyrosine kinase 7 (PTK7) antibody-drug conjugate (ADC) with a topoisomerase I inhibitor as payload (prior therapy with a PTK7 ADC with a non-topoisomerase I inhibitor payload OR non-PTK7 ADC with any payload is permitted). Prior topoisomerase I-based ADCs are not allowed in cohorts A2, B1 or B2. * Any serious unresolved toxicities from prior therapy. * Individual with known or suspected history of uncontrolled central nervous system (CNS) metastases. * Individual with active uncontrolled systemic bacterial, viral, fungal, or parasitic infection. * Significant cardiovascular disease. * Prolongation of QT interval corrected for heart rate using Fridericia's formula (QTcF) \> 470 milliseconds (ms) * History of pneumonitis/interstitial lung disease. * Individuals who are pregnant, breastfeeding, or plan to breastfeed during the trial or within 30 days of the last dose of trial intervention.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Phase 1a-Number of Participants with Dose Limiting Toxicities of LY4175408 | 1 Cycle (21 days) | — |
| Phase 1b-Overall Response Rate (ORR): Percentage of Participants with Best Response of Complete Response (CR) or Partial Response (PR) | Baseline up to approximately 4 years | Per investigator assessed Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Phase 1a and 1b-Pharmacokinetics (PK): Minimum Plasma Concentration (Cmin) of LY4175408 (total antibody, conjugated antibody, free payload) | First 4 cycles (84 days) | — |
| Phase 1a and 1b-PK: Area under the Concentration versus Time Curve (AUC) of LY4175408 (total antibody, conjugated antibody, free payload) | First 4 cycles (84 days) | — |
| Phase 1a-ORR: Percentage of Participants with Best Response of CR or PR | Baseline up to approximately 4 years | Per investigator assessed RECIST 1.1 |
| Phase 1a and 1b-Time to Response (TTR) | Baseline up to approximately 4 years | Per investigator assessed RECIST 1.1 |
| Phase 1a and 1b-Progression-free Survival (PFS) | Baseline up to approximately 4 years | Per investigator assessed RECIST 1.1 |
| Phase 1a and 1b-Disease Control Rate (DCR) | Baseline up to approximately 4 years | Per investigator assessed RECIST 1.1 |
| Phase 1a and 1b-Duration of Response (DOR) | Baseline up to approximately 4 years | Per investigator assessed RECIST 1.1 |
Countries
China, France, Japan, South Korea, Spain, United States
Contacts
CONTACTTrial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
CONTACTPhysicians interested in becoming principal investigators please contact
STUDY_DIRECTORCall 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST)
Eli Lilly and Company
Outcome results
None listed