Brief: BioArctic Partner Submits Leqembi sBLA To FDA
April 2 (Reuters) - BioArctic AB BIOAb.ST :
* SAID ON MONDAY THAT CO'S PARTNER EISAI ANNOUNCED IT HAS
SUBMITTED SUPPLEMENTAL BIOLOGICS LICENSE APPLICATION (SBLA) FOR
MONTHLY LECANEMAB-IRMB (U.S. BRAND NAME: LEQEMBI) INTRAVENOUS
MAINTENANCE DOSING TO THE U.S. FDA
Source text for Workspace: urn:newsml:reuters.com:*:nWkr39n7jl
Further company coverage: BIOAb.ST
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 769 66 00;))
Recent news on BioArctic AB
See all newsBrief: BioArctic And Lilly Sign Research, Collaboration Agreement
Brief: Bioarctic AB Declares Dividend Of Sek 2 Per Share With 1 June 2026 Record Date
Brief: Bioarctic Partner Eisai Presents Leqembi Sales Simulation
Sweden's BioArctic Q1 revenue drops sharply despite higher Leqembi royalties
Brief: BioArctic Q1 Operating Profit SEK 210.8 Million