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NCT02443831
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 .