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

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Biological, Drug, Procedure, Radiation
Study Type: Interventional
Study Phase: Phase 1
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

Eligibility
Participation Requirements
Sex: All
Maximum Age: 24
Healthy Volunteers: f
View:

• 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 equivalent).

⁃ 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 steroid early response (i.e. circulating blast count \>1x10\^9/L following 7 day steroid pre-phase of induction as per national guidelines or equivalent)

⁃ Any patient with t(17,19) TCF3-HLF rearrangement

⁃ High risk 1st relapse (defined as very early (relapse within 18 months of diagnosis) and early relapses (any patient relapsing on therapy or within 6 months of completing treatment) and any relapse with high risk genetics, namely (KMT2A (MLL) rearrangements, low hypodiploidy/near haploidy, t(17;19)(q22;p13)/TCF3-HLF, iAMP21 and t(1;19)(q21;p13)/TCF3- PBX1, t(9;22)(34.1 q11.2)/BCR-ABL1

⁃ Any on therapy relapse in patients age 16-24

⁃ Any relapse of infant ALL

⁃ ALL post ≥ 2nd relapse

⁃ Any refractory relapse of ALL (defined as \> 1% blasts by flow cytometry after a at least 1 cycle of standard chemotherapy)

‣ ALL with MRD \>10-4 prior to planned stem cell transplant

‣ Any relapse of ALL eligible for stem cell transplant but no available HLA matched donor or other contraindication to transplant

‣ Any relapse of ALL after stem cell transplant as long as planned time of CD19+CD22CAR T cell infusion is \> 4 months post-transplant

‣ Early (defined as \< 6 months post-infusion) loss of B cell aplasia or any CD19+CD22+ relapse following CD19CAR T cell therapy with Tisagenlecleucel

• Note patients with isolated CNS relapse meeting one or more of the criteria above are eligible for the study

• Agreement to have a pregnancy test, use adequate contraception (if applicable)

• Written informed consent

Locations
Other Locations
United Kingdom
Great Ormond Street Hospital
RECRUITING
London
University College Hospital
RECRUITING
London
Manchester Royal Children's Hospital
RECRUITING
Manchester
Contact Information
Primary
Aniqa Tasnim
ctc.carpall@ucl.ac.uk
0203 108 4753
Time Frame
Start Date: 2016-04
Estimated Completion Date: 2041-12-31
Participants
Target number of participants: 50
Treatments
Experimental: CD19+CD22 CAR T-cells
Patients meeting the eligibility criteria will have leukapheresis to isolate the blood immune cells used to manufacture the CD19+CD22CAR T-cells. Patients will receive lymphodepletion with low dose total body irradiation, fludarabine and cyclophosphamide prior to infusion of the CD19+CD22CAR T-cells.
Sponsors
Leads: University College, London

This content was sourced from clinicaltrials.gov