Ahead of a key meeting from the US Food and Drug Administration’s scientific advisory panel, briefing notes reveal a broadly positive view of Eisai (TYO: 4523) and Biogen’s (Nasdaq: BIIB) new Alzheimer’s med.
The companies received an Accelerated Approval for Leqembi (lecanemab), an antibody which clears errant plaques of protein in the brain, at the start of the year.
That decision was based on mid-stage data from the ATHENA AD trial, which showed the biologic cleared the plaques and generated a statistically significant reduction in cognitive decline for some patients with early signs of disease.
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