The drugmaker said early results showed that its treatment, lecanemab, reduced patient clinical decline by 27% when compared to a placebo or fake drug after 18 months of the infused treatment.
Eisai announced results late Tuesday from a global study of nearly 1,800 people with early-stage Alzheimer's.
Patients were monitored using a scale that measures mental decline and their ability to do daily activities like getting dressed or feeding themselves.
Eisai Co. Ltd. said it would discuss the full results from the research at a conference in late November. It also plans to publish findings in a peer-reviewed medical journal.
The company is already seeking an accelerated approval from the U.S. Food and Drug Administration, and the agency is expected to decide by early next year. Eisai and Biogen will co-promote the drug.
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