VI-1121 for the Treatment Alzheimer's Disease
Completed · Phase 2 · Has a placebo group
Conditions studied: Alzheimer's Disease
In brief
The purpose of this study is to determine whether VI-1121 is safe, well tolerated, and effective as a daily treatment for Alzheimer's disease that is worsening despite current treatment.
Key facts
- Study ID
- NCT01428362
- Run by
- VIVUS LLC
- People needed
- 61
- Starts
- 2011-08-01
- Expected to finish
- 2013-08-01
- Last updated by the study team
- 2013-12-11
Who can join
Age: 60 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- clinical diagnosis of Alzheimer's disease
- CT or MRI within 2 years prior to study
- stable dose of current Alzheimer's treatment for at least 3 months
You may not qualify if…
- advanced, severe, progressive or unstable disease
- history of cerebrovascular disease or myocardial infarction within 6 months
Where it is running
- Study site — San Francisco, California, United States
- Study site — Santa Monica, California, United States
- Study site — Sunrise, Florida, United States
- Study site — Louisville, Kentucky, United States
- Study site — Las Vegas, Nevada, United States
- Study site — Toms River, New Jersey, United States
- Study site — New Windsor, New York, United States
- Study site — Durham, North Carolina, United States
- Study site — Raleigh, North Carolina, United States
- Study site — Toledo, Ohio, United States
- Study site — Plano, Texas, United States
Full record on ClinicalTrials.gov
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