Brief: UCB Receives U.S. FDA Approval For Bimzelx
Nov 20 (Reuters) - Ucb SA UCB.BR :
* RECEIVES U.S. FDA APPROVAL FOR BIMZELX(BIMEKIZUMAB-BKZX)
AS
FIRST IL-17A AND IL-17F INHIBITOR FOR ADULTS WITH MODERATE TO
SEVERE HIDRADENITIS SUPPURATIVA
* APPROVAL IS SUPPORTED BY DATA FROM TWO PHASE 3 STUDIES, BE
HEARD
I AND BE HEARD II
Source text: ID:nNDL295pXp
Further company coverage: UCB.BR
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 7696600;))
Recent news on UCB SA
See all newsAnalysis: US prices for new drugs fell in 2025 as fewer costly gene therapies were launched
Brief: UCB Announces Data Showing Positive Impact Of Kygevvi In Tk2d Patients
Brief: UCB Completes $2.2 Billion Acquisition Of Candid Therapeutics
Europe Research Roundup: Banca Generali, Ferrari, Prysmian
Barclays downgrades UCB after rally, sees limited upside