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OncoMatch/Clinical Trials/NCT06136364

CD7 CAR-T in Adults With Relapsed or Refractory T-LBL/ALL Clinical Study

Is NCT06136364 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies CAR-T for t-lymphoblastic lymphoma.

Phase 1RecruitingHebei Senlang Biotechnology Inc., Ltd.NCT06136364Data as of May 2026

Treatment: CAR-TTo evaluate the tolerability and safety of SENL101 in patients with relapsed or refractory T-LBL/ALL.

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Extracted eligibility criteria

Cancer type

Acute Lymphoblastic Leukemia

Non-Hodgkin Lymphoma

Biomarker criteria

Required: CD7 overexpression (CD7+ by flow cytometry or IHC)

The tumor cells detected by bone marrow flow cytometry were CD7+ and/or extramedullary lesions were diagnosed as CD7+ by pathological immunohistochemistry at the time of enrollment and screening

Performance status

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

Prior therapy

Min 2 prior lines

Must have received: standard induction chemotherapy

patients who have received at least two courses standard induction regimen and failed to achieve a complete response or complete remission was not achieved after first-line or above salvage treatment

Cannot have received: CAR-T cell therapy

Subjects who have received CAR-T therapy or other gene-modified cell therapy prior to screening

Lab requirements

Blood counts

HGB at least 70g/L, PLT 50x10^9/L, can be transfused

Kidney function

Creatinine <1.5×ULN or creatinine clearance rate(Cockroft-Gault)>50ml/min

Liver function

Total bilirubin <3×ULN; ALT/AST<3×ULN

Cardiac function

Oxygen saturation under air ≥ 92%; LVEF≥50%

Oxygen saturation under air ≥ 92%; LVEF≥50%; Total bilirubin <3×ULN; ALT/AST<3×ULN; Creatinine <1.5×ULN or creatinine clearance rate(Cockroft-Gault)>50ml/min; HGB at least 70g/L,PLT 50x109/L, can be transfused

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

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