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 ...
In the surprise development, the CHMP said that the benefits of the anti-amyloid antibody – which was aiming to become the first disease-modifying drug for Alzheimer's in the EU – are ...