Alzheimer's Disease Safety Extension
A 12-week safety extension study of oral ELND005 for treatment of agitation and aggression in patients with moderate to severe Alzheimer's disease.
Sponsored by Elan Pharma International Limited
The purpose of this study is to determine whether ELND005 is effective in treating symptoms of agitation and aggression in patients with Alzheimer's disease. Eligible patients will have a diagnosis of moderate to severe Alzheimer’s disease and have significant agitation and/or aggression which has not responded to other treatments.
Subjects will be randomly assigned to either the investigational drug or placebo and will be followed for 12 weeks to evaluate the effectiveness and safety of the new drug. About 400 patients will enroll in the study at multiple sites.
More information can be found here.