Universal CD7 CART (uCD7 CART) Cell Injection in the Treatment of Relapsed or Refractory CD7 Positive Hematologic Malignancies: a Prospective, Single-arm, Single-center Clinical Study.

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

The aim of this study was to evaluate the safety and efficacy of universal CD7 CART (uCD7 CART) cells in the treatment of patients with relapsed/refractory CD7-positive hematologic malignancies. In this single-arm, open-label, single-center, Phase 1 clinical trial, two cohorts were set up: (1) relapsed and refractory acute myeloid leukemia (AML) cohort; and (2) relapsed and refractory T lymphoblastic leukemia/lymphoma (T-ALL/LBL) cohort. Each cohort was planned to enroll 4-12 patients. uCD7 CART cells will be administered intravenously to explore the maximum tolerated dose (MTD) of each cohort using a 3+3 dose escalation and rapid titration design.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
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• Age ≥18 and \<70 years, regardless of gender;

• T-ALL/LBL was diagnosed according to the criteria of NCCN Clinical Practice Guidelines for Acute Lymphocytic Leukemia (2020.v1) and T-cell Lymphoma Clinical Practice Guidelines (2020.v1);

• Patients diagnosed with AML with reference to the Guidelines for Diagnosis and Treatment of Adult Acute Myeloid Leukemia (2018 Edition) issued by the Health Commission;

• Cytology confirmed that the tumor cells were CD7 positive.

• Number of blasts in bone marrow ≥5% at screening (bone marrow morphology);

• Complies with the diagnosis of relapsed/refractory AML, including any of the following conditions according to China Guidelines for Diagnosis and Treatment of Relapsed/Refractory Acute Myeloid Leukemia (2021 Edition):

∙ Primary refractory patients who did not achieve CR after two cycles of standard induction chemotherapy;

‣ CR after consolidation chemotherapy, relapse within 12 months;

‣ Relapse 12 months after remission but ineffective after conventional chemotherapy;

‣ 2 or more relapses;

‣ Relapse after hematopoietic stem cell transplantation.

• Meet the diagnosis of relapsed/refractory T-ALL/LBL, including any of the following:

∙ Primary refractory patients who have not achieved complete response after two cycles of standard chemotherapy, or patients who have not achieved complete response after multi-line rescue chemotherapy;

‣ Relapse within \<12 months after complete remission or ≥12 months after complete remission and fail to achieve complete remission induced by 1 or more cycles of standard treatment;

‣ Relapse after hematopoietic stem cell transplantation or relapse after CAR-T therapy at the same target;

• Complies with diagnosis of other relapsed/refractory CD7 positive hematologic malignancies

• Creatine clearance \>60ml/min (Cockcroft and Gault formula); 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;

⁃ Echocardiography showing left ventricular ejection fraction (LVEF) ≥50%;

⁃ Pulse oxygen saturation ≥92%;

⁃ The estimated survival time is more than 3 months;

⁃ ECOG score 0-2;

⁃ Subjects or their legal guardians voluntarily participate in this trial and sign the informed consent form.

Locations
Other Locations
China
Institute of Hematology & Blood Diseases Hospital
RECRUITING
Tianjin
Contact Information
Primary
Jianxiang Wang
wangjx@ihcams.ac
+862223909120
Time Frame
Start Date: 2025-06-28
Estimated Completion Date: 2030-06-28
Participants
Target number of participants: 12
Treatments
Experimental: uCD7 CART
Two cohorts were established: (1) relapsed and refractory acute myeloid leukemia (AML) cohort; and (2) relapsed and refractory T lymphoblastic leukemia/lymphoma (T-ALL/LBL) cohort. A 3+3 dose escalation and rapid titration design was used to explore the maximum tolerated dose (MTD) for each cohort. During the accelerated titration phase, dose-limiting toxicity (DLT) assessments were performed for 1 subject per enrollment and dose escalation was performed until the first DLT event was observed. 3+3 dose escalation CAR-T dose groups were (1) 0.5×10\^6 CART cells/kg; (2)1×10\^6 CART cells/kg;(3) 3×10\^6 CART cells/kg. DLT assessments will be performed first for the first 3 subjects at each dose level (including the last subject at the end of rapid titration) and then for 1 to 3 subjects per enrollment. Therefore, a minimum of 4 and a maximum of 12 patients are expected to be enrolled.
Related Therapeutic Areas
Sponsors
Leads: Institute of Hematology & Blood Diseases Hospital, China

This content was sourced from clinicaltrials.gov

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