NCT06810960Recruiting

A Postmarketing Study of LEQEMBI in South Korean Participants With Alzheimer's Disease

Eisai Korea Inc.

Start Date

2/24/2025

Completion Date

9/30/2029

Summary

The primary purpose of this study is to evaluate safety of LEQEMBI in the real-world clinical setting as reported by events of amyloid-related imaging abnormalities (ARIA)-edema (ARIA-E), ARIA-hemosiderin deposition (ARIA-H), symptomatic ARIA-E, symptomatic ARIA-H, and intracerebral hemorrhage (ICH) greater-than 1 centimeter (cm) in patients treated with LEQEMBI.

Eligibility Criteria

Age Range: 19 years to No maximum

Inclusion Criteria: * Enrolled in JOY-ALZ before the decision to treat with LEQEMBI * The clinical decision to treat with LEQEMBI has already been made * Provides written informed consent for the use of medical information to be shared with Eisai Korea Inc. Exclusion Criteria: * Currently participating in an interventional clinical study

Interventions

OTHER

No Intervention

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Conditions

Alzheimer's Disease

Locations

Eisai Trial Site #1

Nutley, New Jersey 07110

United States

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