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

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

Recruiting
19 years and older
All
Phase N/A
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Overview

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

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

Study details
    Alzheimer's Disease

NCT06810960

Eisai Korea Inc.

15 May 2026

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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