๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-14

A Study of FG-3246 in Participants With Metastatic Castration-Resistant Prostate Cancer (mCRPC) (NCT06842498)

A Phase 2 Dose Optimization Trial Evaluating a CD46-Targeted Antibody-Drug Conjugate (FG-3246) in Patients With Metastatic Castration-Resistant Prostate Cancer

๐ŸŸข Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Kyntra Bio

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

The purpose of this study is to evaluate the safety, efficacy, tolerability, and pharmacokinetics (PK) of FG-3246, a cluster of differentiation 46 (CD46) targeting antibody-drug conjugate (ADC), in the treatment of participants with mCRPC who have progressed following treatment with one prior second-generation androgen receptor signaling inhibitor (ARSI) in any setting and no prior taxane therapy in the mCRPC setting.

Who can join: Review the eligibility criteria below.

Location: Western Regional Medical Center - City of Hope Phoenix Goodyear โ€” Goodyear, Arizona

Age range: 18 Years

๐Ÿงช Interventions in This Study

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 (23 Sites)

  • Western Regional Medical Center - City of Hope Phoenix Goodyear โ€” Goodyear, Arizona
  • HonorHealth Research Institute โ€” Scottsdale, Arizona
  • The University of Arizona Cancer Center - North Campus โ€” Tucson, Arizona
  • VA Greater Los Angeles Healthcare System โ€” Los Angeles, California
  • UCLA Clark Urology Center โ€” Los Angeles, California
  • University of California San Francisco โ€” San Francisco, California
  • New Haven Hospital - Yale Cancer Center โ€” New Haven, Connecticut
  • Bioresearch Partner - Aventura โ€” Aventura, Florida
  • Bioresearch Partner - Hialeah โ€” Hialeah, Florida
  • Biogenix Molecular, LLC โ€” Miami, Florida
  • Winship Cancer Institute, Emory University โ€” Atlanta, Georgia
  • East Jefferson General Hospital Metairie โ€” New Orleans, Louisiana
  • New Mexico Oncology Hematology Consultants, Ltd. โ€” Albuquerque, New Mexico
  • Duke University Medical Center - Duke Cancer Center โ€” Durham, North Carolina
  • University Hospitals Cleveland Medical Center โ€” Cleveland, Ohio
  • Carolina Urologic Research Center โ€” Myrtle Beach, South Carolina
  • Henry-Joyce Cancer Clinic โ€” Nashville, Tennessee
  • University of Texas Southwestern Medical Center โ€” Dallas, Texas
  • Oncology Consultants โ€” Houston, Texas
  • University of Virginia Comprehensive Cancer Center โ€” Charlottesville, Virginia
  • Fred Hutchinson Cancer Center โ€” Seattle, Washington
  • University of Washington Medical Center โ€” Seattle, Washington
  • Northwest Medical Specialties, PLLC - Tacoma โ€” Tacoma, Washington

๐Ÿ“ž Contact the Study Coordinator

Phone: (415) 978-1466

Email: jmoreno@kyntrabio.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†—