πŸ›οΈ Verified NIH Record β€’ Updated 2026-04-02

A Study of CD19 Targeted CAR T Cell Therapy in Adult Patients With Relapsed or Refractory B Cell Acute Lymphoblastic Leukaemia (ALL) (NCT04404660)

An Open-Label, Multi-Centre, Phase Ib/II Study Evaluating the Safety and Efficacy of AUTO1, a CAR T Cell Treatment Targeting CD19, in Adult Patients With Relapsed or Refractory B Cell Acute Lymphoblastic Leukaemia

πŸ”΅ Active, Not Recruiting Phase1 / Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: Autolus Limited

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

This is a Phase 1b/2 study to evaluate the safety and efficacy of autologous T cells engineered with a chimeric antigen receptor (CAR) targeting CD19 in adult patients with relapsed or refractory (r/r) B cell acute lymphoblastic leukemia (ALL).

Who can join: Review the eligibility criteria below.

Location: City of Hope National Medical Center β€” Duarte, California

Age range: 18 Years

πŸ§ͺ Interventions in This Study

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 (34 Sites)

Showing the first 25 of 34 sites.

  • City of Hope National Medical Center β€” Duarte, California
  • University of California San Diego Health (UCSD) β€” La Jolla, California
  • University of California Davis (UC Davis) β€” Sacramento, California
  • University of California San Francisco (UCSF) β€” San Francisco, California
  • Colorado Blood Cancer Institute (CBCI) β€” Denver, Colorado
  • University of Miami β€” Miami, Florida
  • H Lee Moffitt Cancer Center β€” Tampa, Florida
  • Winship Cancer Institute of Emory University β€” Atlanta, Georgia
  • University of Chicago β€” Chicago, Illinois
  • University of Kansas β€” Kansas City, Kansas
  • University of Maryland Medical Center β€” Baltimore, Maryland
  • Dana-Farber Cancer Institute β€” Boston, Massachusetts
  • Mayo Clinic β€” Rochester, Minnesota
  • Washington University School of Medicine β€” St Louis, Missouri
  • University of Nebraska β€” Omaha, Nebraska
  • Memorial Sloan Kettering Cancer Center β€” New York, New York
  • University of Rochester β€” Rochester, New York
  • Cleveland Clinic β€” Cleveland, Ohio
  • TriStar Centennial Medical Center (SCRI) β€” Nashville, Tennessee
  • Baylor Scott & White Research Institute β€” Dallas, Texas
  • MD Anderson Cancer Center β€” Houston, Texas
  • TTI-Methodist (Texas Transplant Institute) (SCRI) β€” San Antonio, Texas
  • The Medical College of Wisconsin β€” Milwaukee, Wisconsin
  • Fundacio' Hospital Universitari Vall d'Hebron β€” Barcelona,
  • Hospital Universitario Virgen del RocΓ­o β€” Seville,

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.

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†—