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OncoMatch/Clinical Trials/NCT07153068

SupCD7 CART for Relapsed or Refractory CD7 Positive Hematologic Malignancies

Is NCT07153068 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies supCD7 CART cells for t lymphoblastic leukemia/lymphoma.

Phase 1/2RecruitingInstitute of Hematology & Blood Diseases Hospital, ChinaNCT07153068Data as of Jun 2026Location: China

Treatment: supCD7 CART cellsThe aim of this study was to evaluate the safety and efficacy of supCD7 CART cells in the treatment of patients with relapsed/refractory CD7-positive hematologic malignancies. In this single-arm, open-label, single-center, Phase Ⅰ+Ⅱ clinical trial, two cohorts were set up: (1) relapsed and refractory AML cohort; and (2) relapsed and refractory T-ALL/LBL cohort. Each cohort was planned to enroll 4-12 patients. SupCD7 CART cells will be administered intravenously to explore the MTD of each cohort using a 3+3 dose escalation and rapid titration design.

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Extracted eligibility criteria

Treatments studied

Other

supCD7 CART cells

Cancer type

Acute Lymphoblastic Leukemia

Non-Hodgkin Lymphoma

Acute Myeloid Leukemia

Biomarker criteria

Required: CD7 positive

Performance status

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

Demographics

Ages ≤ 70

Prior therapy

Cannot have received: systemic chemotherapy

Exception: except for pretreatment

Systemic chemotherapy (except for pretreatment) within 1 week

Cannot have received: monoclonal antibody

For those who have received monoclonal antibody therapy, the last time of monoclonal antibody infusion is less than 5 half-lives or 4 weeks (whichever is shorter) at screening

Cannot have received: donor lymphocyte infusion

Received donor lymphocyte infusion (DLI) within 6 weeks

Lab requirements

Kidney function

creatine clearance >60ml/min (cockcroft and gault formula)

Liver function

serum total bilirubin ≤3 times the upper limit of normal, serum alt and ast ≤5 times the upper limit of normal range for patients without liver invasion

Cardiac function

left ventricular ejection fraction (lvef) ≥50%

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

Frequently asked questions

Is NCT07153068 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior systemic chemotherapy, monoclonal antibody, donor lymphocyte infusion disqualifies patients from enrollment.

Does this trial require CD7?

Yes, CD7 positive is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 70 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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