Condition: Leukemia · Acute Lymphoblastic Leukemia · Sponsor: Stanford University
The primary purpose of this study is to determine safety, feasibility, and the Maximum Tolerated Dose (MTD)/Recommended Phase 2 Dose (RP2D) of CD22 Chimeric Antigen Receptor T-Cell Therapy (CART) cells when administered 28 to 42 days after an infusion of a commercial CAR called Tisagenlecleucel, to children and young adults with relapsed or refractory B-cell leukemia.
This description comes directly from the study's public registry record.
Michelle Fujimoto · (650) 736-0539 · mfujimot@stanford.edu
Always discuss trial participation with your own doctor first.
| Stanford University | Palo Alto, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06408194