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RECRUITING
NCT02443831
PHASE1

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

Sponsor: University College, London

View on ClinicalTrials.gov

Summary

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

Official title: Immunotherapy with CD19+CD22 CAR Redirected T-cells for High Risk/relapsed Paediatric CD19+ and CD22+ Acute Lymphoblastic Leukaemia

Key Details

Gender

All

Age Range

Any - 24 Years

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2016-04

Completion Date

2041-12-31

Last Updated

2025-04-02

Healthy Volunteers

No

Interventions

PROCEDURE

Leukapheresis

Patients will undergo an unstimulated leukapheresis to isolate the required immune cells to produce the CD19+CD22 CAR T-cells

RADIATION

Total Body Irradiation (TBI)

Participants will receive total body irradiation delivered as a single fraction (2Gy) on day -7 prior to CD19+CD22CAR T-cell infusion.

DRUG

Lymphodepletion with Fludarabine

Patients will receive lymphodepleting chemotherapy with iv fludarabine 30 mg/m2 on days -6 to -3 prior to CD19+CD22CAR T-cell infusion.

DRUG

Lymphodepletion with Cyclophosphamide

Patients will receive lymphodepleting chemotherapy with iv cyclophosphamide 0.5 g/m2 on days -6 to -5 prior to CD19+CD22CAR T-cell infusion.

BIOLOGICAL

CD19+CD22 CAR T-cells

Dose level 1: 2 doses of 4 x 10\^5 CD19+CD22 CAR T-cells/kg Dose level 2: 2 doses of 1 x 10\^6 CD19+CD22 CAR T-cells/kg given as a split dose as an intravenous injection through a Hickman line or PICC line (peripherally inserted central catheter) on day 0 and day 14.

Locations (3)

Great Ormond Street Hospital

London, United Kingdom

University College Hospital

London, United Kingdom

Manchester Royal Children's Hospital

Manchester, United Kingdom