NCT02650414Active, not recruitingPhase 1

CD22 Redirected Autologous T Cells for ALL

Pilot Study of Autologous Anti-CD22 Chimeric Antigen Receptor Redirected T Cells in Pediatric Patients With Chemotherapy Resistant Or Refractory Acute Lymphoblastic Leukemia

Source: ClinicalTrials.gov · Last updated 7 Jul 2026

Brief summary (registry, in English)

This is a pilot study to determine the feasibility and safety of a single dose of autologous T cells expressing CD22 chimeric antigen receptors expressing tandem TCR-ζ and 4-1BB signaling domains (CART22/CART22-65s cells) in pediatric and young adult subjects with relapsed or refractory B cell acute lymphoblastic leukemia.

Status (registry): Active, not recruiting
Phase (registry): Phase 1
Study type: Interventional
Enrollment: 41 (estimated)
First submitted: 22 Dec 2015
Start date: 13 Jan 2016
Primary completion date: Dec 2037
Lead sponsor: University of Pennsylvania
Diseases: Acute lymphoblastic leukaemia, Chronic lymphocytic leukaemia, Childhood cancers
NCT number: NCT02650414

What you commit to

Study type: Interventional · Phase 1
Planned participants: 41
From 13 Jan 2016 to the primary completion date, Dec 2037
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 immunosuppressant medications. Recent or current use of inhaled steroids or physiologic replacement with hydrocortisone is not exclusionary.
Receipt of a prior investigational study agent within 4 weeks prior to screening visit. \*Note - patients who have received anti-CD19 CART cells (e.g., CART19/CTL019) on an investigational study where cell infusion occurred greater than 4 weeks before the screening visit are NOT excluded.

Other illness

Active hepatitis B or active hepatitis C.
HIV Infection.
Active acute or chronic graft-versus-host disease (GVHD) requiring systemic therapy.
CNS3 disease that is progressive on therapy, or with CNS parenchymal lesions that might increase the risk of CNS toxicity.

Other

Pregnant or nursing (lactating) women.

Criteria the registry did not label

Signed informed consent form must be obtained prior to any study procedure.
Relapsed or refractory B-cell ALL:
- 2nd or greater relapse OR
- Any marrow or extramedullary relapse after allogeneic HSCT and ≥ 6 months from SCT at infusion OR
- Any marrow relapse after CAR-modified T cell therapy OR
- Refractory disease defined as having not achieved a CR after \> 2 chemotherapy regimens OR
- Patients with Ph+ ALL are eligible if they are intolerant to or have failed tyrosine kinase inhibitor therapy OR
- Ineligible for allogeneic SCT because of:
- Comorbid disease ii. Other contraindications to allogeneic SCT conditioning regimen iii. Lack of suitable donor iv. Prior SCT v. Declines allogeneic SCT as a therapeutic option after documented discussion, with expected outcomes, about the role of SCT with a BMT physician not part of the study team g. Patients with CNS3 disease will be eligible if CNS disease is responsive to therapy (at infusion, must meet criteria in Section 5.2)
Documentation of CD22 tumor expression in bone marrow, other tumor biopsy, CSF or peripheral blood by flow cytometry (or a recent marrow in the case of refractory disease). If the patient has received CD22-directed therapy (i.e., inotuzumab), then the marrow or other sample should be obtained after this therapy to show CD22 expression.
Adequate organ function defined as:
- A serum creatinine based on age/gender as follows:
- Maximum Serum Creatinine (mg/dL) Age 1 to \< 2 years Male 0.6 Female 0.6 Age 2 to \< 6 years Male 0.8 Female 0.8 Age 6 to \< 10 years Male 1.0 Female 1.0 Age 10 to \< 13 years Male 1.2 Female 1.2 Age 13 to \< 16 years Male 1.5 Female 1.4 Age ≥ 16 years Male 1.7 Female 1.4
- Adequate liver function
- ALT \< 500 U/L ii. Bilirubin \<3x upper limit of normal iii. ALT and/or bilirubin that exceed these ranges is acceptable if, in the opinion of the investigator (or by liver biopsy), the abnormalities are directly related to ALL infiltration of the liver c. Must have a minimum level of pulmonary reserve defined as ≤ Grade 1 dyspnea, pulse oxygen \> 92% on room air; DLCO \> 40% (corrected for anemia) if PFTs are clinically appropriate as determined by the treating investigator d. Left Ventricle Shortening Fraction (LVSF) ≥ 28% or Ejection Fraction (LVEF) ≥ 40% confirmed by ECHO/MUGA; in cases where quantitative assessment of LVEF is not possible, a statement by the cardiologist that the ECHO shows qualitatively normal ventricular function will suffice.
Evidence of disease by standard morphologic or by MRD criteria. If the results of a historical biopsy (obtained at the time of the patient's most recent relapse) are available, this does not need to be repeated at screening.
Age 1-29 years.
Adequate performance status (Lansky or Karnofsky score ≥50).
Subjects of reproductive potential must agree to use acceptable birth control methods.

Age in the registry: 1 year 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.

Site	City	Country	Site status
Children's Hospital of Philadelphia Coordinator of this site? Confirm its status	Philadelphia	United States	Unknown status

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