Condition: Alzheimer's Disease · Sponsor: Eisai Korea Inc.
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.
This description comes directly from the study's public registry record.
Eisai Korea Inc. Medical department Serena SoYoun Kwon · +82-2-3451-5533 · s-kwon@eisaikorea.com
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| Eisai Trial Site #1 | Nutley, New Jersey, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06810960