drugset / Trial / NCT05169684

A Study of BMS-986218 or BMS-986218 Plus Nivolumab in Combination With Docetaxel in Participants With Metastatic Castration-resistant Prostate Cancer

NCT05169684 ↗

Phase 2 Terminated 10 enrolled Bristol-Myers Squibb
RandomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to assess the safety, efficacy, tolerability, and toxicity of docetaxel alone, in combination with BMS-986218, or in combination with nivolumab plus BMS-986218 in men who have metastatic castration-resistant prostate cancer (mCRPC) that progressed after novel antiandrogen therapy and have not received chemotherapy for mCRPC.

Timeline

Start
2022-02-14
Primary completion
2023-12-06
Completion
2023-12-06

Outcome

Outcome not reported

Stopped (Business): “Business objectives have changed”

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986218 Monoclonal antibody — —
Subject Docetaxel Small molecule — —
Subject Nivolumab Monoclonal antibody — —