Skip to content
Study details
Enrolling now

A Study to Assess BMS-986460 in Participants With Metastatic Castration-resistant Prostate Cancer

Bristol-Myers Squibb
NCT IDNCT06067841ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Ages

18+

Sex

Male only

Locations

8 sites in CA, FL, MA +4

What this study is about

This Phase 1 study is focused on people with metastatic castration resistant prostate cancer. The primary outcome being measured is Number of deaths.

Simplified from trial records by PatientMatch.

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Standard assignment

Assignment is predetermined by the study protocol.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Number of deaths, Number of participants with AEs leading to study intervention discontinuation, Number of participants with AEs meeting protocol defined dose limiting toxicity (DLT) criteria, Number of participants with adverse events (AEs), Number of participants with serious adverse events (SAEs)

Secondary: Area under the plasma concentration-time curve (AUC), Duration of response (DOR), Maximum concentration (Cmax), Number of participants with a confirmed prostate specific antigen decline of ≥ 30% from baseline response rate, Time of maximum concentration (Tmax)

Body systems

Oncology