drugset / Trial / NCT03956680

An Investigational Immunotherapy Study of BMS-986301 Alone or in Combination With Nivolumab, and Ipilimumab in Participants With Advanced Solid Cancers

NCT03956680 ↗

Phase 1 Completed 54 enrolled Bristol-Myers Squibb
NaSequentialOpen-labelTreatment

Summary

The main purpose of this study is to characterize the safety, tolerability, dose limiting toxicities, best route of administration, maximum tolerated dose, maximum administered dose, or alternative dose of BMS-986301 alone or in combination with nivolumab and ipilimumab in participants with cancers that have failed to respond to T cell checkpoint inhibiting antibodies.

Timeline

Start
2019-03-26
Primary completion
2024-04-17
Completion
2024-04-24

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986301 Unknown — Intramuscular
Subject Ipilimumab Monoclonal antibody — —
Subject Nivolumab Monoclonal antibody — —

Indications

No indication recorded.