drugset / Trial / NCT04570839

COM701 in Combination With BMS-986207 and Nivolumab in Subjects With Advanced Solid Tumors.

NCT04570839

Phase 1/2 Completed 48 enrolled Compugen Ltd Bristol-Myers Squibb · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a phase 1/2 open label sequential dose escalation and cohort expansion study evaluating the safety, tolerability and preliminary antitumor activity of COM701 in combination with BMS-986207 and nivolumab in patients with advanced solid tumors.

Timeline

Start
2020-08-31
Primary completion
2024-05-15
Completion
2024-05-15

Drugs

EvaluationDrugModalityDoseRoute
Subject COM701 Monoclonal antibody Intravenous
Background Nivolumab Monoclonal antibody Intravenous
Background RENVISTOBART Monoclonal antibody Intravenous