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| Therapy Name | BEAM-201 |
| Synonyms | |
| Therapy Description |
BEAM-201 comprises allogeneic T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CD7 and to harbor mutations in TRAC, CD7, CD52, and PDCD1, which potentially induces killing of tumor cells expressing CD7 (Blood (2024) 144 (Supplement 1): 4838, NCI Drug Dictionary). |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| BEAM-201 | BEAM 201|BEAM201 | CD7 Immune Cell Therapy 4 | BEAM-201 comprises allogeneic T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CD7 and to harbor mutations in TRAC, CD7, CD52, and PDCD1, which potentially induces killing of tumor cells expressing CD7 (Blood (2024) 144 (Supplement 1): 4838, NCI Drug Dictionary). |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
|---|---|---|---|---|---|---|
| NCT05885464 | Phase Ib/II | BEAM-201 | A Study Evaluating the Safety and Efficacy of BEAM-201 in Relapsed/Refractory T-Cell Acute Lymphoblastic Leukemia (T-ALL) or T-Cell Lymphoblastic Lymphoma (T-LL) | Active, not recruiting | USA | 0 |
| NCT06934382 | Phase I | BEAM-201 | Anti-CD7 CAR-T Cells in Relapsed/Refractory T-Cell Acute Lymphoblastic Leukemia or Lymphoma (24CT015) | Recruiting | USA | 0 |