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| Therapy Name | Cyclophosphamide + Fludarabine + NY-ESO-1 TCR/IL-15 NK cells |
| Synonyms | |
| Therapy Description | |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| Cyclophosphamide | Cytoxan | CPM | Chemotherapy - Alkylating 18 | Cytoxan (cyclophosphamide) is an alkylating agent, which inhibits DNA replication (NCI Drug Dictionary). Cytoxan (cyclophosphamide) is FDA approved in multiple hematological malignancies, breast cancer, neuroblastoma, ovarian cancer, and retinoblastoma (NCI Drug Dictionary). |
| Fludarabine | Fludara | FAMP|Fludarabine phosphate | Flurdara (fludarabine) is converted to 2-fluoro-ara-ATP intracellularly, which potentially inhibits DNA polymerase alpha, ribonucleotide reductase and DNA primase, leading to decreased DNA synthesis and reduced tumor growth (NCI Drug Dictionary) | |
| NY-ESO-1 TCR/IL-15 NK cells | Allogeneic anti-NY-ESO-1 TCR-transduced IL-15-expressing CB-derived NK cells | NY-ESO-1 TCR/IL-15 NK cells are allogeneic natural killer (NK) cells derived from cord blood that are engineered to express a T-cell receptor (TCR) targeting NY-ESO-1 and to express IL-15, which potentially induce toxicity in tumor cells expressing NY-ESO-1 (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 |
|---|---|---|---|---|---|---|
| NCT06083883 | Phase I | Cyclophosphamide + Fludarabine + NY-ESO-1 TCR/IL-15 NK cells | Phase I/Ib Study of NK Expressing an Affinity-enhanced T-cell Receptor (TCR) Against the NY-ESO-1 | Recruiting | USA | 0 |
| NCT06066359 | Phase Ib/II | Cyclophosphamide + Fludarabine + NY-ESO-1 TCR/IL-15 NK cells | Phase I/II Trial of Cord Blood-Derived NK Cells Genetically Engineered With NY-ESO-1 TCR/IL-15 Cell Receptor for Relapsed/Refractory Multiple Myeloma | Recruiting | USA | 0 |