Magrolimab - Forty Seven
Alternative Names: 5F9; GS-4721; Hu5F9 G4; Magrolimab - Forty-Seven/Stanford-University; ONO 7913Latest Information Update: 08 Jul 2026
At a glance
- Originator Stanford University
- Developer Forty Seven; Gilead Sciences; M. D. Anderson Cancer Center; Merck KGaA; Merck Sharp & Dohme; National Cancer Institute (USA); Ono Pharmaceutical; Roche; Stanford University; University of California at San Francisco
- Class Antineoplastics; Immunotherapies; Monoclonal antibodies
- Mechanism of Action Antibody-dependent cell cytotoxicity; CD47 antigen inhibitors; Macrophage stimulants; T lymphocyte stimulants
-
Orphan Drug Status
Yes - Acute myeloid leukaemia; Myelodysplastic syndromes
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Discontinued Acute myeloid leukaemia; Brain cancer; Colorectal cancer; Cutaneous B-cell lymphoma; Diffuse large B cell lymphoma; Follicular lymphoma; Head and neck cancer; Hodgkin's disease; Lymphoma; Multiple myeloma; Myelodysplastic syndromes; Neuroblastoma; Non-Hodgkin's lymphoma; Osteosarcoma; Ovarian cancer; Pancreatic cancer; Solid tumours; Triple negative breast cancer
Most Recent Events
- 08 Jul 2026 Discontinued - Phase-I for Colorectal cancer (Combination therapy, Inoperable/Unresectable, Late-stage disease, First-line therapy, Recurrent) in Japan (IV)
- 08 Jul 2026 Discontinued - Phase-I for Pancreatic cancer (Combination therapy, First-line therapy, Metastatic disease) in Japan (IV)
- 08 Jul 2026 Discontinued - Phase-I/II for Colorectal cancer (Combination therapy, Late-stage disease, Second-line therapy or greater) in USA (IV)