A Plan on Investigation and Collection of Aricept Safety Information With a Dose Increase on Alzheimer's Disease Patients
NCT02158910 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2231
Last updated 2017-03-07
Summary
The purpose of the study is for investigation and collection of Aricept safety information with a dose increase on Alzheimer's disease patients.
Conditions
Interventions
- DRUG
-
Aricept
5 mg Aricept increasing dose to 10 mg Aricept, or 10 mg Aricept increasing dose to 23 mg Aricept
Sponsors & Collaborators
-
Eisai Korea Inc.
lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-03-31
- Primary Completion
- 2016-06-30
- Completion
- 2016-06-30
Countries
- South Korea
Study Locations
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