Condition: Alzheimer's Disease · Sponsor: Eisai Co., Ltd.
The primary purpose of this study is to investigate the characteristics of amyloid related imaging abnormalities (ARIA) and investigate the treatment continuation status (e.g., continuation, interruption) after the onset of ARIA in routine clinical practice in participants treated with lecanemab.
This description comes directly from the study's public registry record.
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| Eisai trial site 2 | Hiroshima, Japan | Recruiting |
| Eisai trial site 3 | Kyoto, Japan | Recruiting |
| Eisai trial site 1 | Tokyo, Japan | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06322667