A 36-Week Safety Extension Study of ELND005 as a Treatment for Agitation and Aggression in Alzheimer's Disease
Status: | Terminated |
---|---|
Conditions: | Alzheimer Disease, Psychiatric |
Therapuetic Areas: | Neurology, Psychiatry / Psychology |
Healthy: | No |
Age Range: | 50 - Any |
Updated: | 4/21/2016 |
Start Date: | January 2013 |
End Date: | August 2015 |
A 36-Week Safety Extension Study of Oral ELND005 for Treatment of Agitation and Aggression in Patients With Moderate to Severe Alzheimer's Disease
To evaluate the safety and tolerability of ELND005 treatment with up to 48 weeks exposure,
in Moderate to Severe AD patients with agitation and aggression.
in Moderate to Severe AD patients with agitation and aggression.
Inclusion Criteria:
- Complete Week 12 visit of AG201
- Both patient and study partner/caregiver are willing and able to participate in all
scheduled evaluations and complete all required tests
Exclusion Criteria:
- Is currently using any other investigational or experimental drugs or devices
- Has significant worsening of medical conditions or dementia such that it may preclude
completion of this safety extension study
We found this trial at
39
sites
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