Stopped: Genmab has decided to terminate the GEN1286 program due to an unfavorable benefit-risk profile not supporting further development.
The purpose of this trial is to evaluate the safety, tolerability, pharmacokinetics (PK), anti-tumor activity and immunogenic potential of GEN1286 in participants with advanced solid tumors. This trial consists of 2 parts: * Part A: Dose escalation and dose level expansion * Part B: Tumor-specific expansion with dose optimization
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Number of Participants With Adverse Events (AEs)
Timeframe: From first dose until 12 months post last dose of study drug or withdrawal of consent, death, or study closure, whichever occurs first (Up to approximately 3 years 9 months)
Number of Participants With Dose Limiting Toxicities (DLTs)
Timeframe: During first cycle (Cycle length=21 days)