πŸ›οΈ Verified NIH Record β€’ Updated 2026-08-10

Spearhead 1 Study in Subjects With Advanced Synovial Sarcoma or Myxoid/Round Cell Liposarcoma (NCT04044768)

A Phase 2 Single Arm Open-Label Clinical Trial of ADP-A2M4 SPEARβ„’ T Cells in Subjects With Advanced Synovial Sarcoma or Myxoid/Round Cell Liposarcoma

πŸ”΅ Active, Not Recruiting Phase2 πŸ“‹ Clinical Research Protocol Sponsor: USWM CT, LLC

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

This is a study to investigate the efficacy and safety of ADP-A2M4 in HLA-A\*02 eligible and MAGE-A4 positive subjects with metastatic or inoperable (advanced) Synovial Sarcoma (Cohort 1, 2 and 3 ) or MRCLS (Cohort 1) .

Who can join: Review the eligibility criteria below.

Location: City of Hope β€” Duarte, California

Age range: 10 Years to 75 Years

πŸ§ͺ Interventions in This Study

  • afamitresgene autoleucel (previously ADP-A2M4) (GENETIC)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

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

πŸ“ All Participating Trial Locations (26 Sites)

Showing the first 25 of 26 sites.

  • City of Hope β€” Duarte, California
  • Stanford Cancer Center β€” Palo Alto, California
  • University of Colorado β€” Aurora, Colorado
  • Mayo Clinic Jacksonville β€” Jacksonville, Florida
  • Moffitt Cancer Center β€” Tampa, Florida
  • Northwestern University Robert H. Lurie Comprehensive Cancer Center β€” Chicago, Illinois
  • National Cancer Institute β€” Bethesda, Maryland
  • Massachusetts General Hospital β€” Boston, Massachusetts
  • Dana Farber Cancer Institute β€” Boston, Massachusetts
  • University of Michigan β€” Ann Arbor, Michigan
  • Washington University School of Medicine β€” St Louis, Missouri
  • Memorial Sloan-Kettering Cancer Center β€” New York, New York
  • Ohio State University β€” Columbus, Ohio
  • Vanderbilt β€” Nashville, Tennessee
  • MD Anderson Cancer Center β€” Houston, Texas
  • Fred Hutch β€” Seattle, Washington
  • Medical College of WI Froedtert Hospital β€” Milwaukee, Wisconsin
  • Princess Margaret Cancer Centre β€” Toronto, Ontario
  • Centre Leon Berard β€” Lyon,
  • Hospital Haut Leveque, CHU Bordeaux β€” Pessac,
  • Gustave Roussy Cancer Center β€” Villejuif,
  • Hospital Universitari Vall D'Hebron β€” Barcelona, Catalonia
  • Start Madrid-FJD, FundaciΓ³n Jimѐnez DΓ­az β€” Madrid,
  • Hospital Universitario Virgen del Rocio β€” Seville,
  • UCLH Cancer Clinical Trials Unit β€” London,

πŸ“ž Contact the Study Coordinator

Phone: (800) 826-4673

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

πŸ’° 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 Β§ 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.

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πŸ’‘ 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.
πŸ›οΈ View Official NIH Record β†—