BIOA•prnewswire•
Leqembi® Iqlik™ (lecanemab-irmb) supplemental Biologics License Application regarding subcutaneous starting dose granted Priority Review by the US FDA
Summary
STOCKHOLM, Jan. 25, 2026 /PRNewswire/ -- BioArctic AB's (publ) (STO: BIOA B) partner Eisai announced today that the supplemental Biologics License Application (sBLA) for Leqembi Iqlik subcutaneous autoinjector (SC-AI) as a weekly starting dose has been granted Priority Review by the U.S....
Original Article
Read the full article from the original source for complete details and context.
Read Full ArticleArticle published on January 26, 2026 by prnewswire