CARPALL: Immunotherapy With CD19+CD22 CAR T-cells for CD19+ and CD22+ Acute Lymphoblastic Leukaemia

This study aims to evaluate the safety, efficacy and duration of response of CD19+CD22 Chimeric Antigen Receptor (CAR) redirected autologous T-cells in children with high risk, relapsed CD19+ and CD22+ acute lymphoblastic leukaemia

Trial Details

NCT ID
NCT02443831
Phase
PHASE1
Sponsor
University College, London
Status
RECRUITING
Cancer Type
Acute Lymphoblastic (ALL) Leukemia
Interventions
  • Leukapheresis
  • Total Body Irradiation (TBI)
  • Lymphodepletion with Fludarabine
  • Lymphodepletion with Cyclophosphamide
  • CD19+CD22 CAR T-cells
Locations (sample)
  • London, United Kingdom|51.50853,-0.12574
  • London, United Kingdom|51.50853,-0.12574
  • Manchester, United Kingdom|53.48095,-2.23743

Key Eligibility Criteria

  • Children and young adults (age 24 years or younger) with high risk/relapsed CD19+ and CD22+ acute lymphoblastic leukaemia with:
  • Resistant disease (\>5% blasts) at end of ALLTogether-1 protocol or equivalent induction
  • ALL with persisting high level MRD at 2nd time point of frontline national protocol (currently MRD \>10-4 at week 9 ALLTogether-1 Protocol or equiv…
  • High risk infant ALL (age \< 6 months at diagnosis with MLL gene rearrangement and either presenting white cell count \> 300 x 10\^9/L or poor ster…

For full eligibility, visit ClinicalTrials.gov.

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