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NCT04557436CompletedPhase 1

TT52CAR19 Therapy for B-cell Acute Lymphoblastic Leukaemia (B-ALL)

Phase 1, Open Label Study of CRISPR-CAR Genome Edited T Cells (PBLTT52CAR19) in Relapsed /Refractory B Cell Acute Lymphoblastic Leukaemia

Source: ClinicalTrials.gov · Last updated 7 Mar 2024

Brief summary (registry, in English)

PBLTT52CAR19 modified T cells are allogenic engineered human T cells (defined as TT52CAR19 +TCRαβ-) prepared for the treatment of CD19+ B cell leukaemia. The cells are from healthy adult volunteer donors and are not HLA-matched. They have been transduced to express and anti-CD19 chimeric antigen receptor (CAR19) using a lentiviral vector that also incorporates CRISPR guides for genome editing of CD52 and TRAC loci in the presence of transiently provided Cas9. Recognition by TT52CAR19 T cells mediates eradication of CD19+ leukaemia and other CD19+ B cells through T cell mediated cytotoxicity. This study aims to apply PBLTT52CAR19 T cells to secure molecular remission in children with relapsed/refractory B-ALL ahead of programmed allogeneic stem cell transplantation. The cells are to be used in a time-limited manner for their anti-leukaemia effects and then depleted by standard pre- transplant conditioning.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
9 (actual)
First submitted
15 Sept 2020
Start date
12 Aug 2020
Primary completion date
5 Mar 2024
Lead sponsor
Great Ormond Street Hospital for Children NHS Foundation Trust
NCT number
NCT04557436

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 9
  • From 12 Aug 2020 to the primary completion date, 5 Mar 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Presence of donor-specific anti-HLA antibodies directed against PBLTT52CAR19
  • GvHD requiring systemic therapy
  • Systemic steroid therapy prednisolone \>0.5mg/kg/day
  • Uncontrolled viraemia is defined as rising viral loads on two consecutive occasions despite antiviral therapy.
  • Risk of pregnancy or non-compliance with contraception (if applicable). Girls of childbearing potential must have been tested negative in a pregnancy test within 14 days prior to inclusion.
  • Intrathecal methotrexate within 4 weeks or intrathecal chemotherapy (e.g Ara-C) within 2 weeks of lymphodepletion
  • Less than 2 half-lives from prior therapy with immune checkpoint pathway modifiers to lymphodepletion
  • Prior CAR19 therapy known to be associated with ≥Grade 3 cytokine release syndrome (CRS) or ≥Grade 3 drug-related CNS toxicity

Other illness

  • Evidence of disease progression after cytoreduction
  • Uncontrollable CNS leukaemia or neurological symptoms defined as CNS grade 3 (per National Comprehensive Cancer National guidelines). Patients developing grade 3 CNS disease at any time after enrolment will be excluded.
  • Known hypersensitivity to any of the test materials or related compounds
  • Active bacterial, fungal, or viral infection not controlled by a standard of care anti-microbial or anti-viral treatment. Uncontrolled bacteraemia/ fungaemia is defined as the ongoing detection of bacteria/fungus on blood cultures despite antibiotic or anti-fungal therapy.

Other

  • Patients/parents unwilling to undergo a follow-up for 15 years
  • Foreseeable poor compliance to the study procedures
  • CD19-negative B-cell leukaemia
  • Absence of suitable HLA matched or mismatched donor
  • Weight \< 6 kgs
  • Lactating female participants unwilling to stop breastfeeding

Who the study is looking for

  • Patients with relapsed (second or subsequent bone marrow relapse or bone marrow relapse after allo-SCT) or refractory (not achieving an initial complete response (CR) after 2 cycles of standard chemotherapy) CD19-positive B-acute lymphoblastic leukaemia
  • Morphologically confirmed with leukemic blasts in the bone marrow or a quantifiable MRD load of 1x10-4 (by multiparameter flow cytometry and/or quantitative polymerase chain reaction)
  • Eligible and fit for allogeneic hematopoietic stem cells transplantation with suitable donor available
  • Estimated life expectancy ≥ 12 weeks
  • Lansky (age \< 16 years at the time of assent/consent) or Karnofsky (age ≥ 16 years at the time of assent/consent) performance status ≥ 50 Eastern Cooperative Oncology Group ECOG performance status \< 2

Age in the registry: 6 months to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Great Ormond Street Hospital
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.