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Vemircopan

Alternative Names: vemircopan, ach-0145228, ach0145228, ach 0145228, ach-5228, ach5228, ach 5228, alxn-2050, alxn 2050, alxn2050
Latest Update: 2024-10-02
Latest Update Note: Clinical Trial Update

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

Map of Global Clinical Trials for Vemircopan

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

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