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A Randomized Study to Evaluate FK962 in Subjects With Mild to Moderate Alzheimer's Disease

2014-08-27 03:54:12 | BioPortfolio

Summary

The purpose of this study is to evaluate the safety and efficacy of five fixed dosage levels of FK962 or placebo for 24 weeks in subjects with mild to moderate Alzheimer's disease. Patient visits are every six weeks with limited efficacy measurements at week 6 and 18.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Conditions

Alzheimer's Disease

Intervention

FK962

Location

Investigational Site
Phoenix
Arizona
United States
85013

Status

Terminated

Source

Astellas Pharma Inc

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:54:12-0400

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