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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

2026-05-22

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 low-dose total body irradiation delivered as a single fraction on day -7 prior to CD19+CD22CAR T-cell infusion.

DRUG

Lymphodepletion with Fludarabine

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

DRUG

Lymphodepletion with Cyclophosphamide

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

BIOLOGICAL

CD19+CD22 CAR T-cells

1 dose of CD19+CD22 CAR T-cells given as an intravenous injection through a Hickman line or PICC line (peripherally inserted central catheter) on day 0.

Locations (3)

Great Ormond Street Hospital

London, United Kingdom

University College Hospital

London, United Kingdom

Manchester Royal Children's Hospital

Manchester, United Kingdom