A Brief Study To Evaluate The Safety, Tolerability, And Blood Levels Of Multiple Doses Of PF-044467943 Or Placebo In Combination With Donepezil In Subjects With Mild To Moderate Alzheimer's Disease
Completed · Phase 1 · Has a placebo group
Conditions studied: Alzheimer's Disease
In brief
The purpose of the study is to evaluate the safety of PF-04447943 when given in combination with donepezil in subjects who have Alzheimer's Disease. The study will also evaluate the absorption and distribution of both PF-04447943 and donepezil.
Key facts
- Study ID
- NCT00988598
- Run by
- Pfizer
- People needed
- 15
- Starts
- 2009-10-26
- Expected to finish
- 2010-07-05
- Last updated by the study team
- 2020-11-19
Who can join
Age: 55 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects must have Alzheimer's dementia with a Mini Mental State Examination score between 18-26, inclusive.
- Subjects must have a reliable caregiver.
- Subjects must be on Aricept
- Memantine is allowed if subjects are on a stable dose
- Subjects must be in reasonably good health, based on medical history, physical examination, vital signs, and ECG, with no serious or unstable disease within the past 3 months.
You may not qualify if…
- Subjects with clinically significant heart disease cannot participate.
- Subjects with a past or current history of seizures cannot participate.
Where it is running
- Glendale Adventist Medical Center — Glendale, California, United States
- University of Florida - Center for Clinical Trials Research — Gainesville, Florida, United States
- MD Clinical — Hallandale, Florida, United States
Full record on ClinicalTrials.gov
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