The Food and Drug Administration (FDA) has accepted the Biologics License Application (BLA) for subcutaneous (SC) maintenance dosing of lecanemab-irmb for the treatment of Alzheimer disease (AD) in ...
It is anticipated that people with AD-specific pathologic alterations may develop dementia at different rates in the absence of disease-modifying treatments. Slow amyloid-β (Aβ) protein aggregation, ...
The agency expects to issue a decision by Aug. 31, and it is slated to decide on maintenance dosing for an intravenous form of the drug later this month.