Eisai (ESAIY) and Biogen (BIIB) announced that the Committee for Medicinal Products for Human Use of the European Medicines Agency has reaffirmed its positive opinion by consensus for the anti-Abeta monoclonal antibody lecanemab, adopted in November 2024. Following CHMP’s reaffirmation, after having considered the additional information requested by the European Commission, the EC will resume the decision-making process for lecanemab’s marketing authorization.
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