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Therapy Name | Cyclophosphamide + Fludarabine + Letetresgene autoleucel |
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) | |
Letetresgene autoleucel | GSK3377794|GSK-3377794|GSK 3377794|NY-ESO-1-c259T | Letetresgene autoleucel (GSK3377794) are autologous T-cells engineered to express a T-cell receptor that recognizes the cancer testis antigen, CTAG1B (NY-ESO-1), which may induce an immune response against CTAG1B and/or CTAG2 (LAGE-1)-expressing cancer cells (PMID: 26193344, PMID: 36075914). |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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NCT03967223 | Phase II | Cyclophosphamide + Fludarabine + Letetresgene autoleucel | Master Protocol to Assess the Safety and Antitumor Activity of Genetically Engineered T Cells in NY-ESO-1 and/or LAGE-1a Positive Solid Tumors (IGNYTE-ESO) | Active, not recruiting | USA | NLD | ITA | GBR | FRA | ESP | CAN | 0 |