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
π©Ί 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
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π 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,
π 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.
π° 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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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.