๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-17

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 (NCT06764485)

A Phase 3, Two-part, Randomized, Open-label, Adaptive Study Comparing BMS-986365 Versus Investigator's Choice of Therapy Comprising Either Docetaxel or Second Androgen Receptor Pathway Inhibitor (ARPI), in Participants With Metastatic Castration-resistant Prostate Cancer (mCRPC) - rechARge

๐ŸŸข Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Celgene

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The purpose of this study is to compare the efficacy and safety of BMS-986365 versus the investigator's choice of therapy in participants with Metastatic Castration-resistant Prostate Cancer.

Who can join: Review the eligibility criteria below.

Location: Central Alabama Research โ€” Birmingham, Alabama

Age range: 18 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (281 Sites)

Showing the first 25 of 281 sites.

  • Central Alabama Research โ€” Birmingham, Alabama
  • Banner MD Anderson Cancer Center โ€” Gilbert, Arizona
  • Local Institution - 0370 โ€” Anaheim, California
  • Moores Cancer Center โ€” La Jolla, California
  • Cancer and Blood Specialty Clinic โ€” Los Alamitos, California
  • Local Institution - 0364 โ€” Los Angeles, California
  • California Pacific Medical Center โ€” San Francisco, California
  • San Francisco VA Health Care System โ€” San Francisco, California
  • Local Institution - 0458 โ€” Santa Rosa, California
  • Rocky Mountain Regional VA Medical Center โ€” Aurora, Colorado
  • Rocky Mountain Cancer Centers, LLP โ€” Denver, Colorado
  • Colorado Clinical Research โ€” Lakewood, Colorado
  • Sibley Memorial Hospital โ€” Washington D.C., District of Columbia
  • Lakeland Regional Cancer Center โ€” Lakeland, Florida
  • Local Institution - 0077 โ€” Athens, Georgia
  • Northwestern Memorial Hospital โ€” Chicago, Illinois
  • The University of Kansas Cancer Center - Westwood โ€” Westwood, Kansas
  • Wichita Urology Group โ€” Wichita, Kansas
  • Chesapeake Urology โ€” Baltimore, Maryland
  • Johns Hopkins Hospital โ€” Baltimore, Maryland
  • James M Stockman Cancer Institute โ€” Frederick, Maryland
  • Local Institution - 0104 โ€” Minneapolis, Minnesota
  • Local Institution - 0049 โ€” Las Vegas, Nevada
  • Thomas Jefferson University, Kennedy Health Alliance โ€” Sewell, New Jersey
  • University of New Mexico Comprehensive Cancer Center โ€” Albuquerque, New Mexico

๐Ÿ“ž Contact the Study Coordinator

Phone: (855) 907-3286

Email: Clinical.Trials@bms.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—