RecruitingEarly Phase 1NCT07144020
Donor Derived CD117 CAR-T Cells in the Treatment of R/R Acute Myeloid Leukemia
Donor Derived CD117 CAR-T Cells in the Treatment of Relapsed/Refractory Acute Myeloid Leukemia
Sponsor
Zhejiang University
Enrollment
50 participants
Start Date
Sep 5, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
A Clinical Study on the Safety and Effectiveness of Donor Derived CD117 CAR-T Cell in the treatment of Relapsed/Refractory Acute Myeloid Leukemia
Eligibility
Min Age: 18 Years
Inclusion Criteria12
- \. Patients with a histologically or immunophenotypically confirmed diagnosis of CD117-positive Acute Myeloid Leukemia (AML).
- \. Diagnosis must meet the 2016 WHO classification criteria for AML and fulfill the definitions for relapsed or refractory disease per the \*Chinese Guidelines for the Diagnosis and Management of Relapsed/Refractory Acute Myeloid Leukemia (2017 Edition)\*, with no available suitable standard therapeutic options or registered clinical trials.
- a). Relapsed AML: Defined as the reappearance of leukemic blasts in the peripheral blood, bone marrow blast count \>5% (when assessed morphologically, after excluding regenerative changes post-consolidation chemotherapy), or development of extramedullary disease after achieving a Complete Remission (CR).
- b). Refractory AML (meeting at least one criterion): Failure to achieve CR following two cycles of standard induction therapy in newly diagnosed patients; relapse within 12 months after CR following consolidation therapy; relapse beyond 12 months that fails to respond to conventional salvage chemotherapy; ≥2 relapses; or persistent extramedullary leukemia.
- \. Presence of \>5% bone marrow blasts (by morphology) and/or \>1% (by flow cytometric analysis).
- \. Total bilirubin ≤1.5 × ULN (≤51 μmol/L) ALT and AST ≤3 × ULN Serum creatinine ≤1.5 × ULN (≤176.8 μmol/L)
- \. Left ventricular ejection fraction (LVEF) ≥50% as assessed by echocardiography.
- \. Oxygen saturation ≥92% on room air.
- \. Life expectancy ≥3 months.
- \. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2.
- \. For patients of childbearing potential: Agreement to use highly effective contraception from screening, throughout the study treatment period, and for at least 6 months after the cell infusion (due to unknown risks to the fetus).
- \. Voluntary participation, understanding of the study procedures, and provision of written informed consent by the patient or their legally authorized representative.
Exclusion Criteria9
- \. Patients with the history of epilepsy or other CNS disease;
- \. Patients with prolonged QT interval time or severe heart disease;
- \. Active infection with no cure;
- \. Active infection of hepatitis B virus or C virus ;
- \. Before using any gene therapy products;
- \. The proiferation rate is less than 5 times response to CD3/CD28 co-stimulation signal;
- \. Suffering from other uncontrolled diseases that the researchers consider unsuitable for joining;
- \. Infected with AIDS virus;
- \. Any situation that researchers believe may increase the risk to the subjects or interfere with the trial results.
Interventions
BIOLOGICALCD117 CAR T-cells
Each subject receive CD117 CAR T-cells by intravenous infusion
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07144020
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