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| Therapy Name | Flotetuzumab |
| Synonyms | |
| Therapy Description |
Flotetuzumab (MGD006) is a humanized bispecific antibody that targets both CD123 (IL32A) and CD23, which may lead to anti-leukemic activity (Blood 2017 130(Suppl 1):637, PMID: 32493790, PMID: 32929488). |
| Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
|---|---|---|---|---|
| Flotetuzumab | MGD006|S80880 | CD123 (IL3RA) Antibody 14 | Flotetuzumab (MGD006) is a humanized bispecific antibody that targets both CD123 (IL32A) and CD23, which may lead to anti-leukemic activity (Blood 2017 130(Suppl 1):637, PMID: 32493790, PMID: 32929488). |
| 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 |
|---|---|---|---|---|---|---|
| NCT03739606 | Phase II | Flotetuzumab | Flotetuzumab in Treating Patients With Recurrent or Refractory CD123 Positive Blood Cancer | Withdrawn | 0 | |
| NCT04582864 | Phase II | Flotetuzumab | Flotetuzumab for Relapsed Acute Myeloid Leukemia (AML) Following Allogeneic Hematopoietic Cell Transplantation (Allo-HCT) | Terminated | USA | 0 |
| NCT02152956 | Phase Ib/II | Flotetuzumab | Safety Study of MGD006 in Relapsed/Refractory Acute Myeloid Leukemia (AML) or Intermediate-2/High Risk MDS | Terminated | USA | NLD | ITA | ISR | GBR | FRA | ESP | DEU | 0 |
| NCT05506956 | Phase I | Flotetuzumab | Post-transplant Flotetuzumab for AML | Completed | USA | 0 |