AstraZeneca’s Fasenra Wins FDA Approval for Rare Vasculitis
Company Announcements

AstraZeneca’s Fasenra Wins FDA Approval for Rare Vasculitis

AstraZeneca (GB:AZN) has released an update.

AstraZeneca’s drug Fasenra has received FDA approval in the U.S. for treating eosinophilic granulomatosis with polyangiitis (EGPA), a rare, life-threatening immune-mediated vasculitis. Grounded in the successful MANDARA trial, Fasenra showed that nearly 60% of patients achieved remission, and 41% could cease oral corticosteroid use, offering a significant new treatment option for the approximately 15,000 U.S. patients with this rare disease.

For further insights into GB:AZN stock, check out TipRanks’ Stock Analysis page.

Related Articles
TheFlyAIM reports preliminary data in Phase 1b/2 study of Ampligen, Imfinzi
TheFlyAstraZeneca’s Fasenra approved in U.S. to treat adults with EGPA
Looking for investment ideas? Subscribe to our Smart Investor newsletter for weekly expert stock picks!
Get real-time notifications on news & analysis, curated for your stock watchlist. Download the TipRanks app today! Get the App