A Safety and Efficacy Study Evaluating Dimebon (Latrepirdine) in Patients With Moderate to Severe Alzheimer's Disease
NCT00954590 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 89
Last updated 2016-09-27
Summary
The purpose of this study is to determine if Dimebon is safe and effective in patients with moderate to severe Alzheimer's disease.
Conditions
- Moderate to Severe Alzheimer
Interventions
- DRUG
-
Dimebon (latrepirdine)
20 mg orally three times daily
- DRUG
-
Placebo orally three times daily
Sponsors & Collaborators
- collaborator INDUSTRY
-
Medivation, Inc.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-10-31
- Primary Completion
- 2010-08-31
Countries
- Chile
- United Kingdom
Study Locations
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