drugset / Trial / NCT07120607
Allogeneic CD7 CAR γδ T Cells Therapy Recurrent/Refractory Leukemia
NaSingle-groupOpen-labelTreatment
Summary
CD7 is highly expressed in T-cell acute lymphoblastic leukemia (T-ALL) and T-cell lymphoma. Approximately 10-30% of cute myeloid leukemia(AML) patients exhibit CD7 expression, particularly in early myeloid progenitor cell-derived AML (e.g., M0/M1 subtypes), mixed-phenotype acute leukemia (MPAL), and AML with high-risk genetic abnormalities (such as TP53 mutations or complex karyotypes). CD7-positive AML patients typically have poor prognosis, poor response to standard chemotherapy, and shorter overall survival (OS). Targeted CD7 cell therapies may represent a promising direction for the treatment of these diseases.
Timeline
- Start
- 2025-08-18
- Primary completion
- 2026-12-31
- Completion
- 2027-12-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CD7 CAR-γδT cell | Cell therapy | 1e+08 cells | Intravenous |
| Subject | CD7 CAR-γδT cell | Cell therapy | 3e+08 cells/kg | Intravenous |
| Subject | CD7 CAR-γδT cell | Cell therapy | 6e+08 cells | Intravenous |
| Background | Cyclophosphamide | Other / unclassified | 500 mg/m2 | Intravenous |
| Background | Cyclophosphamide | Other / unclassified | 1000 mg/m2 | Intravenous |
| Background | Fludarabine | Small molecule | 30 mg/m2 | Intravenous |
| Background | Fludarabine | Small molecule | 50 mg/m2 | Intravenous |