drugset / Trial / NCT07223047

A Study to Evaluate the Safety, Tolerability, and Efficacy of BMS-986523 Alone and in Combination With Anti-Cancer Agents in Participants With Advanced Solid Malignancies

NCT07223047

Phase 1/2 Recruiting 252 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and efficacy of BMS-986523 alone and in combination with anti-cancer agents in participants with advanced solid malignancies

Timeline

Start
2025-11-25
Primary completion
2028-10-13
Completion
2028-10-13

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986523 Unknown
Subject Cetuximab Monoclonal antibody
Subject Gemcitabine Small molecule
Subject Paclitaxel Small molecule
Subject Pembrolizumab Monoclonal antibody