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| Therapy Name | ADI-270 |
| Synonyms | |
| Therapy Description |
ADI-270 comprises allogeneic T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CD70 and containing a dominant negative form of the TGFBR2, which potentially increases antitumor immune activity against CD70-expressing tumors (Journal for ImmunoTherapy of Cancer 2024;12). |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| ADI-270 | ADI270|ADI 270 | CD70 Immune Cell Therapy 11 | ADI-270 comprises allogeneic T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CD70 and containing a dominant negative form of the TGFBR2, which potentially increases antitumor immune activity against CD70-expressing tumors (Journal for ImmunoTherapy of Cancer 2024;12). |
| 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 |
|---|---|---|---|---|---|---|
| NCT06480565 | Phase Ib/II | ADI-270 Cyclophosphamide + Fludarabine | A Phase 1/2 Trial of ADI-270 in CcRCC | Active, not recruiting | USA | 0 |