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Therapy Name | CB-012 |
Synonyms | |
Therapy Description |
CB-012 are allogeneic T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CLEC12A (CLL-1) and genomically edited to resist rejection and immunosuppression, potentially leading to enhanced CLL1-dependent cytotoxicity (Cancer Res (2023) 83 (7_Supplement): 3201). |
Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
---|---|---|---|---|
CB-012 | CB-012 are allogeneic T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CLEC12A (CLL-1) and genomically edited to resist rejection and immunosuppression, potentially leading to enhanced CLL1-dependent cytotoxicity (Cancer Res (2023) 83 (7_Supplement): 3201). |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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NCT06128044 | Phase I | CB-012 Cyclophosphamide + Fludarabine | CRISPR-Edited Allogeneic Anti-CLL-1 CAR-T Cell Therapy in Patients With Relapsed/Refractory Acute Myeloid Leukemia (AMpLify) | Recruiting | USA | 0 |