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NCT05674175RecruitingPhase 1/2

Co-administration of CART22-65s and huCART19 for B-ALL

Use of Autologous Anti-CD22 CAR T Cells (CART22-65s) Co-administered With Humanized Anti-CD19 CAR T Cells (huCART19) in Children and Young Adults With Relapsed or Refractory B-ALL

Source: ClinicalTrials.gov · Last updated 27 Mar 2026

Brief summary (registry, in English)

This study will evaluate the safety and efficacy of administering two CAR T cell products, huCART19 and CART22-65s, in children with advanced B cell Acute Lymphoblastic Leukemia (B-ALL).

Status (registry)
Recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
93 (estimated)
First submitted
6 Dec 2022
Start date
25 Jan 2023
Primary completion date
1 Jul 2028
Lead sponsor
Stephan Grupp MD PhD
NCT number
NCT05674175

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 93
  • From 25 Jan 2023 to the primary completion date, 1 Jul 2028
  • 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

  • Concurrent use of systemic steroids or immunosuppression at the time of cell infusion or cell collection, or a condition, in the treating physician's opinion, that is likely to require steroid therapy or immunosuppression during collection or after infusion. Steroids for disease treatment at times other than cell collection or at the time of infusion are permitted. Use of physiologic replacement hydrocortisone or inhaled steroids is permitted as well.

Other illness

  • Active hepatitis B or active hepatitis C
  • HIV infection
  • Active acute or chronic Graft Vs. Host Disease requiring systemic therapy
  • Central nervous system disease that is progressive on therapy, or with Central nervous system parenchymal lesions that might increase the risk of central nervous system toxicity.
  • Uncontrolled active infection

Other

  • Pregnant or nursing (lactating) women

Who the study is looking for

  • Signed informed consent form
  • Patients with documented CD19+ and/or CD22+ ALL/LLy:
    • Cohort A: Patients with relapsed or refractory ALL/LLy:
    • Cohort B: Patients with poor response to prior B cell directed engineered cell therapy
  • Patients with prior or current history of Central Nervous System 3 disease will be eligible if Central Nervous System disease is responsive to therapy
  • Documentation of CD19 and/or CD22 tumor expression in bone marrow, peripheral blood, Cerebrospinal fluid, or tumor tissue by flow cytometry at the time of last detectable disease. If the patient has experienced a relapse after CD19-directed and/or CD22-directed therapy, flow cytometry should be evaluated after this therapy to demonstrate CD19 and/or CD22 expression.
  • Age 0-29 years
  • Adequate organ function
  • Adequate performance status defined as Lanksy or Karnofsky performance score ≥50.
  • Subjects of reproductive potential must agree to use acceptable birth control methods.

Age in the registry: - to 29 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
Children's Hospital of Philadelphia
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesRecruiting

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