🏛️ Verified NIH Record • Updated 2026-05-21

Study With [225Ac]Ac-FL-020 in mCRPC Participants (NCT06492122)

A Phase 1, First-in-Human, Open-label Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of [225Ac]Ac-FL-020 in Participants With mCRPC.

🟢 Recruiting Phase1 💊 Investigational Drug / Biologic Sponsor: Full-Life Technologies UK Limited

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this study is to evaluate the safety, therapeutic effect, and pharmacokinetics of \[225Ac\]Ac-FL-020 in participants with metastatic castration-resistant prostate cancer (mCRPC).

Who can join: Review the eligibility criteria below.

Location: City of Hope Medical Center — Duarte, California

Age range: 18 Years

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (11 Sites)

  • City of Hope Medical Center — Duarte, California
  • Chao Family Comprehensive Cancer Center — Irvine, California
  • University of Stanford — Stanford, California
  • University Hospital of Cleveland — Cleveland, Ohio
  • University of Virginia Cancer Center — Charlottesville, Virginia
  • Princess Alexandra Hospital — Brisbane,
  • Genesiscare Murdoch — Murdoch,
  • MacQuarie University Clinical Trial Unit — Sydney,
  • Beijing Cancer Hospital — Beijing,
  • Renji Shanghai Hospital — Shanghai,
  • Ankara Üniversitesi Tıp Fakültesi Cebeci Hastanesi Nükleer Tıp Anabilim Dalı — Ankara,

📞 Contact the Study Coordinator

Phone: (973) 727-3254

Email: clinicaltrials@t-full.com

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

💰 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 § 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.

💡 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.
🏛️ View Official NIH Record ↗