Brief: Grifols Gets FDA Approval For New Fibrinogen Concentrate, Fesiltytm
Dec 19 (Reuters) - Grifols SA GRLS.MC: RECEIVES US FDA APPROVAL FOR NEW FIBRINOGEN CONCENTRATE, FESILTYTM (FIBRINOGEN, HUMAN-CHMT) FESILTY EXPECTED TO BE AVAILABLE IN THE U.S. WITHIN THE FIRST HALF OF 2026 CONCENTRATE, FESILTY APPROVED IN THE U.S. FOR ACUTE BLEEDING EPISODES IN PEDIATRIC AND ADULT PATIENTS WITH CONGENITAL FIBRINOGEN DEFICIENCY Source text Further company coverage: GRLS.MC (Gdansk Newsroom) ((Gdansk.newsroom@thomsonreuters.com; +48 58 769 66 00;))
Recent news on Grifols
See all newsSpanish stocks - Factors to watch on Nov 3
Brief: Grifols Approves Interim Dividend Of €0.15/Shr Payable On Dec 4
Brief: Grifols Q3 Group Profit €162 Mln
Refile: Grifols says Canada plasma license suspension has no impact on ongoing operations
Brief: Health Canada Suspends Licence Of Grifols Site In Winnipeg - Globe And Mail