Actively Recruiting
A Post Marketing Study in Participants With Early Alzheimer's Disease Treated With Lecanemab
Led by Eisai Co., Ltd. · Updated on 2026-01-23
5000
Participants Needed
3
Research Sites
202 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
A Post Marketing Study in Participants With Early Alzheimer's Disease Treated With Lecanemab
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants treated with lecanemab in routine clinical practice
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Eisai trial site 2
Hiroshima, Japan
Actively Recruiting
2
Eisai trial site 3
Kyoto, Japan
Actively Recruiting
3
Eisai trial site 1
Tokyo, Japan
Actively Recruiting
Research Team
E
Eisai Inquiry Service.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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