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Phase 1/2 Study of UCART22 in Patients With Relapsed or Refractory CD22+ B-cell Acute Lymphoblastic Leukemia (BALLI-01)

RecruitingPhase 1, Phase 2Ages 15 Years - 50 YearsAllCellectis S.A.
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In plain words

What the trial is, and whether it could suit you

This is a first-in-human, open-label, dose escalation and expansion study of UCART22 administered intravenously to patients with relapsed or refractory B-cell acute Lymphoblastic Leukemia (B-ALL). The purpose of this study is to evaluate the safety and clinical activity of UCART22 and determine the Maximum Tolerated Dose (MTD) and Recommended Phase 2 Dose (RP2D)

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * B-ALL blast cells expressing CD22 * Diagnosed with R/R B-ALL * Prior therapy must include at least one standard chemotherapy regimen and at least one salvage regimen Exclusion Criteria: -Prior cellular therapy or investigational cellular or gene therapy within 90 days prior to enrollment
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What it tests

  • UCART22
  • CLLS52
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Where

19 sites
University of California, Los Angeles (UCLA) - Medical Center
Los Angeles, United States
University of Colorado - Aurora Cancer Center
Aurora, United States
Sarah Cannon - Colorado Blood Cancer Institute
Denver, United States
University of Chicago
Chicago, United States
Dana Farber Cancer Institute
Boston, United States
Roswell Park Comprehensive Cancer Center
Buffalo, United States
Memorial Sloan Kettering Cancer Center (MSKCC) David H. Koch Center for Cancer Care at Memorial Sloan Kettering Cancer Center
New York, United States
Weill Medical College of Cornell University
New York, United States

โ€ฆand 11 more on ClinicalTrials.gov.

๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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