Alexion FDA Friday, December 21, 2018 0.00 Neutral

FDA Approves ULTOMIRIS — Alexion Pharmaceuticals Inc.

# FDA Approves Alexion Pharmaceuticals' ULTOMIRIS for Complement-Mediated Disorders Alexion Pharmaceuticals Inc. received FDA approval for ULTOMIRIS (ravulizumab), an intravenous complement inhibitor, positioning the company to compete in the rare disease market and potentially expand its market share beyond its existing complement-targeting therapies. The approval of this long-acting C5 inhibitor is expected to drive significant revenue growth for Alexion in treating paroxysmal nocturnal hemoglobinuria and other rare blood disorders.

View original filing at SEC.gov →
AI-generated summary for informational purposes only. Always verify against the original filing. Not investment advice. BriefTape is not a registered investment adviser.

Get real-time financial news in your trading bot or app

GET FREE KEY — 10,000 calls/day