drugset / Trial / NCT06618287

A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of BMS-986507 Combinations in Adult Participants With Advanced Solid Tumors

NCT06618287

Phase 1/2 Recruiting 416 enrolled Bristol-Myers Squibb
RandomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, drug levels, and preliminary efficacy of BMS-986507 combinations in adult participants with advanced solid tumors.

Timeline

Start
2025-02-04
Primary completion
2031-02-26
Completion
2031-02-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Izalontamab Brengitecan Unknown
Subject Nivolumab Monoclonal antibody
Subject Osimertinib Small molecule
Subject Pembrolizumab Monoclonal antibody
Subject Pumitamig Protein / enzyme biologic