Product Description
Mafosfamide is a synthetic oxazaphosphorine derivative with antineoplastic properties. Mafosfamide alkylates DNA, forming DNA cross-links and inhibiting DNA synthesis. Although closely related to cyclophosphamide, mafosfamide, unlike cyclophosphamide, does not require hepatic activation to generate its active metabolite 4-hydroxy-cyclophosphamide; accordingly, mafosfamide is potentially useful in the intrathecal treatment of neoplastic meningitis. (Sourced from: https://pubchem.ncbi.nlm.nih.gov/compound/Mafosfamide)
Mechanisms of Action: STING Inhibitor
Novel Mechanism: Yes
Modality: Small Molecule
Route of Administration: Intravenous
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Baylor College of Medicine
Company Location:
Company CEO:
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 1: Spinal Cancer|Leukemia|Brain Cancer|Bone Cancer|Lymphoma|Gastrointestinal Cancer|Leukemia, Experimental|Brain Stem Cancer
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
BB'98 | N/A |
Completed |
Brain Cancer |
2005-12-01 |
|
J0563 | N/A |
Completed |
Acute Myeloid Leukemia |
None |
|
H3241 | P1 |
Completed |
Spinal Cancer|Brain Cancer|Bone Cancer|Lymphoma|Gastrointestinal Cancer|Leukemia, Experimental |
None |
|
90-C-0095 | P1 |
Completed |
Leukemia|Lymphoma |
None |