Anti-Ly6E Exatecan ADC M7437 in Advanced Solid Tumors
NCT07311603 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 138
Last updated 2025-12-31
Summary
The purpose of this first-in-human (FIH) study is to evaluate the safety, tolerability, Pharmacokinetics (PK), and preliminary clinical activity of M7437 in participants with locally advanced or metastatic solid tumors with known Ly6E expression, including non-small cell lung cancer (NSCLC), triple-negative breast cancer (TNBC), epithelial ovarian carcinoma (EOC), squamous cell carcinoma of the head and neck (SCCHN), pancreatic ductal adenocarcinoma (PDAC), and gastric cancer (GC).
Conditions
Interventions
- DRUG
-
M7437
Participants will receive M7437 as an intravenous infusion at a dose corresponding to their assigned cohort. Dose escalation will occur between cohorts, with 3-4 participants enrolled at each dose level before proceeding to the next higher dose.
- DRUG
-
M7437
Participants will receive M7437 at a dose that was determined as recommended dose for expansion (RDE) in Part 1.
Sponsors & Collaborators
-
Merck KGaA, Darmstadt, Germany
collaborator INDUSTRY -
Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany
lead INDUSTRY
Principal Investigators
-
Medical Responsible · Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-01-02
- Primary Completion
- 2028-09-20
- Completion
- 2029-03-28
- FDA Drug
- Yes
Countries
- Germany
Study Locations
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