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| Therapy Name | ARD103 |
| Synonyms | |
| Therapy Description |
ARD103 are T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CLEC12A (CLL1) that contains CD28 transmembrane and co-stimulatory domains and a CD3zeta activation domain, which may inhibit growth of CLL1-expressing tumor cells (JCO Global Oncol 2023 9: Supplement_1, 119). |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| ARD103 | ARD 103|ARD-103 | ARD103 are T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CLEC12A (CLL1) that contains CD28 transmembrane and co-stimulatory domains and a CD3zeta activation domain, which may inhibit growth of CLL1-expressing tumor cells (JCO Global Oncol 2023 9: Supplement_1, 119). |
| 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 |
|---|---|---|---|---|---|---|
| NCT06680752 | Phase Ib/II | Cyclophosphamide + Fludarabine ARD103 | Clinical Study of ARD103 CAR-T Therapy for Patients With R/R AML or MDS | Recruiting | USA | 0 |