Patient Guide: A Study to Compare the Efficacy and Safety of BMS-986365 Versus the Investigator's Choice of Therapy in Participants With Metastatic Castration-resistant Prostate Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 248 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06764485
Status: 🟢 Enrolling Now
Condition: Metastatic Castration-resistant Prostate Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 248 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Gilbert, Arizona
  • • Anaheim, California
  • • And 245 more locations

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A Study to Compare the Efficacy and Safety of BMS-986365 Versus the Investigator's Choice of Therapy in Participants With Metastatic Castration-resistant Prostate Cancer - Join Clinical Trial NCTNCT06764485

How to Join This Clinical Trial - NCTNCT06764485

Learn how to participate in this PHASE3 trial studying an investigational therapy for Metastatic Castration-resistant Prostate Cancer. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Metastatic Castration-resistant Prostate Cancer. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Metastatic Castration-resistant Prostate Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06764485 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 248 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35209 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Gilbert, Arizona 85234 - United States

Status: RECRUITING

Clinical Research Site

Anaheim, California 92801 - United States

Status: RECRUITING

Clinical Research Site

La Jolla, California 92093 - United States

Status: RECRUITING

Clinical Research Site

Los Alamitos, California 90720 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90048 - United States

Status: WITHDRAWN

Clinical Research Site

San Francisco, California 94115 - United States

Status: RECRUITING

Clinical Research Site

San Francisco, California 94121 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Denver, Colorado 80218 - United States

Status: RECRUITING

And 238 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Metastatic Castration-resistant Prostate Cancer:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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