Anti-amyloid monoclonal that achieved 27% slowing on CDR-SB; led to traditional FDA approval July 2023. Defined the post-amyloid AD-disease-modifying era.

Details

nct_id
NCT03887455
phase
phase_3
status
completed
domain
alzheimers
indication
Early Alzheimer's Disease
intervention
Lecanemab (anti-amyloid monoclonal)
sponsor
Eisai / Biogen
n_enrolled
1795
primary_endpoint
CDR-Sum of Boxes change from baseline at 18 months
Raw fields (1)
metadata
{}

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