drugset / Trial / NCT07459543

A Study To Assess the Safety, and Tolerability of Nivolumab + Relatlimab Fixed-Dose Combination (FDC) In Untreated, Unresectable or Metastatic Melanoma Participants In India

NCT07459543

Phase 4 Not yet recruiting 30 enrolled Bristol-Myers Squibb
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and tolerability of Nivolumab + Relatlimab Fixed-Dose Combination (FDC) in untreated, unresectable or metastatic melanoma participants in India

Timeline

Start
2026-11-15
Primary completion
2029-05-26
Completion
2029-05-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody
Subject Relatlimab Monoclonal antibody

Indications