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Sponsors and Collaborators: |
Astellas Pharma Inc Astellas Pharma US, Inc. |
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Information provided by: | Astellas Pharma Inc |
ClinicalTrials.gov Identifier: | NCT00087724 |
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.
Condition | Intervention | Phase |
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Alzheimer's Disease |
Drug: FK962 |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Phase 2 Study to Evaluate the Safety and Efficacy of FK962 in Subjects With Mild to Moderate Alzheimer's Disease |
Ages Eligible for Study: | 50 Years to 90 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study Director: | Use Central Contact | Astellas Pharma US, Inc. |
Study ID Numbers: | 03-0-189 |
Study First Received: | July 12, 2004 |
Last Updated: | July 20, 2006 |
ClinicalTrials.gov Identifier: | NCT00087724 |
Health Authority: | United States: Food and Drug Administration |
Delirium, Dementia, Amnestic, Cognitive Disorders Mental Disorders Alzheimer Disease Central Nervous System Diseases Neurodegenerative Diseases |
Brain Diseases Dementia Cognition Disorders Delirium |
Nervous System Diseases Tauopathies |