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| Therapy Name | PRGN-3007 |
| Synonyms | |
| Therapy Description |
PRGN-3007 are T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting ROR1, membrane-bound IL-15, and kill switch genes, which potentially induce cytotoxicity against ROR1-expressing tumor cells and reduce tumor growth (Blood (2021) 138 (Supplement 1): 1694). |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| PRGN-3007 | PRGN3007|PRGN 3007|UltraCAR-T Cells PRGN-3007 | ROR1 Immune Cell Therapy 5 | PRGN-3007 are T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting ROR1, membrane-bound IL-15, and kill switch genes, which potentially induce cytotoxicity against ROR1-expressing tumor cells and reduce tumor growth (Blood (2021) 138 (Supplement 1): 1694). |
| 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 |
|---|---|---|---|---|---|---|
| NCT05694364 | Phase I | PRGN-3007 Cyclophosphamide Cyclophosphamide + Fludarabine | Dose Escalation/Dose Expansion Study of PRGN-3007 UltraCAR-T Cells in Patients With Advanced Hematologic and Solid Tumor Malignancies | Active, not recruiting | USA | 0 |