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| Therapy Name | Allogeneic CD19-CD28-CD3-zeta CAR-T cells + Mycophenolate mofetil + Sirolimus |
| Synonyms | |
| Therapy Description | |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| Allogeneic CD19-CD28-CD3-zeta CAR-T cells | Allogeneic 19-28z CAR T-cells|Allogeneic CD19-28z CAR T Cells | CD19 Immune Cell Therapy 72 | Allogeneic CD19-CD28-CD3-zeta CAR-T cells are allogeneic T-lymphocytes engineered to express a chimeric antigen receptor (CAR) targeting CD19 linked to the CD28 co-stimulatory receptor and CD3zeta, which potentially induce toxicity in CD19-expressing tumor cells (NCI Drug Dictionary). | |
| Mycophenolate mofetil | Cellcept | RS-61443 | Cellcept (mycophenolate mofetil) is metabolized to mycophenolic acid, which interferes with proliferation of B- and T-lymphocytes, resulting in immunosuppresion (PMID: 32228535). | |
| Sirolimus | Rapamune | Rapamycin | mTORC1 Inhibitor 9 | Rapamune (sirolimus) binds to the FKBP-12 to generate an immunosuppressive complex that binds and allosterically inhibits mTOR (PMID: 25261369). Rapamune (sirolimus) is FDA approved for the prevention of renal transplant rejection and for patients with lymphangioleiomyomatosis (FDA.gov). |
| 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 |
|---|---|---|---|---|---|---|
| NCT07162038 | Phase I | Cyclophosphamide + Fludarabine Allogeneic CD19-CD28-CD3-zeta CAR-T cells + Mycophenolate mofetil + Sirolimus | Phase I Trial Integrating HLA-Haploidentical Anti-CD19 CAR-T Cells With Post-Transplantation Cyclophosphamide-Based HLA-Haploidentical Hematopoietic Cell Transplantation | Recruiting | USA | 0 |