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OncoMatch/Clinical Trials/NCT03938987

Anti-CD19, Dual Co-stimulatory (4-1BB, CD3ζ) Chimeric Antigen Receptor T-cells in Patients With Relapsed/Refractory Aggressive Lymphoma or Acute Lymphoblastic Leukemia (ALL)

Is NCT03938987 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies autologous CD19-directed chimeric antigen receptor (CAR) T-cells for relapsed non hodgkin lymphoma.

Phase 1/2RecruitingUniversity of AlbertaNCT03938987Data as of May 2026

Treatment: autologous CD19-directed chimeric antigen receptor (CAR) T-cellsAutologous, unselected CD3+ lymphocytes collected from apheresis, transfected with a lentiviral vector containing a 2nd generation chimeric antigen receptor (CAR) consisting of a scFv recognizing CD19 and dual co-stimulatory intracellular signaling domains (4-1BB and CD3ζ).

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Extracted eligibility criteria

Cancer type

Hodgkin Lymphoma

Non-Hodgkin Lymphoma

Acute Lymphoblastic Leukemia

Biomarker criteria

Required: CD19 positive

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Min 2 prior lines

Must have received: systemic therapy

At least 2 prior systemic therapies

Cannot have received: immunotherapy directly targeting T-cells

Exception: anti-thymocyte globulin [ATG]

Prior treatment with immunotherapy directly targeting T-cells (except anti-thymocyte globulin [ATG])

Cannot have received: CD19-directed antibody-based therapies

Exception: blinatumomab

Prior treatment with ... CD19-directed antibody-based therapies (except blinatumomab)

Cannot have received: gene therapy products

Prior treatment with ... other gene therapy products

Cannot have received: investigational drug/anti-cancer therapy

Received any investigational drug/anti-cancer therapy within 30 days

Cannot have received: donor lymphocyte infusion

Donor lymphocyte infusion (DLI) within 4 weeks prior to leukapheresis

Cannot have received: salvage or debulking chemotherapy

Salvage or debulking chemotherapy within 1 week prior to blood collection for CAR T-cell product manufacture

Lab requirements

Kidney function

Cockroft-Gault creatinine clearance > 50 mL/min unless directly related to malignant disease being treated for on study

Liver function

total bilirubin < 1.5x ULN; and AST/ALT < 3x ULN unless directly related to malignant disease being treated for on study

Adequate renal function (defined as Cockroft-Gault creatinine clearance > 50 mL/min) and hepatic function (total bilirubin < 1.5x ULN; and AST/ALT < 3x ULN) unless directly related to malignant disease being treated for on study

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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