Product Description
Vemircopan is an orally bioavailable inhibitor of complement factor D (FD; CFD), a serineprotease that cleaves complement factor B, with potential complement system inhibiting activity. (Sourced from: https://pubchem.ncbi.nlm.nih.gov/compound/Vemircopan)
Mechanisms of Action: CFD Inhibitor
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: AstraZeneca
Company Location: CAMBRIDGE X0 CB2 0AA
Company CEO: Pascal Soriot
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic: Argentina, Australia, Brazil, China, Germany, Israel, Italy, Korea, Mexico, Peru, Serbia, South Korea, Spain, Taiwan, Thailand, Turkey, United Kingdom, United States, Unknown Location
Active Clinical Trial Count: 11
Highest Development Phases
Phase 2: Glomerulonephritis|IgA Nephropathy|Kidney Diseases|Lupus Nephritis|Myasthenia Gravis
Phase 1: Healthy Volunteers
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
ALXN2050-NEPH-201 | P2 |
Unknown Status |
IgA Nephropathy|Lupus Nephritis |
2028-07-31 |
|
ALXN2050-NEPH-201 | P2 |
Active, not recruiting |
IgA Nephropathy|Lupus Nephritis |
2026-07-11 |
|
ALXN2050-NEPH-201 | P2 |
Active, not recruiting |
Glomerulonephritis|Kidney Diseases|Lupus Nephritis|IgA Nephropathy |
2026-06-30 |
|
- | P2 |
Active, not recruiting |
Myasthenia Gravis |
2025-01-10 |