Efficacy and Safety Study of ELND005 as a Treatment for Agitation and Aggression in Alzheimer's Disease
Status: | Completed |
---|---|
Conditions: | Alzheimer Disease, Neurology, Psychiatric |
Therapuetic Areas: | Neurology, Psychiatry / Psychology |
Healthy: | No |
Age Range: | 50 - 95 |
Updated: | 4/21/2016 |
Start Date: | November 2012 |
End Date: | May 2015 |
A Prospective, Randomized, Double-Blind, Placebo-Controlled, Phase 2 Efficacy and Safety Study of Oral ELND005 for Treatment of Agitation and Aggression in Patients With Moderate to Severe Alzheimer's Disease
The primary purpose of this study is to determine whether ELND005 is effective in treating
symptoms of agitation and aggression in patients with Alzheimer's disease
symptoms of agitation and aggression in patients with Alzheimer's disease
Inclusion Criteria:
- Diagnosis of Probable AD according to the National Institute on Aging- Alzheimer's
Association (NIA-AA) guidelines (McKhann et al 2011).
- MMSE score of 5 to 24 (inclusive) at the Screening Visit.
- Has clinically significant agitation/aggression defined as Neuropsychiatric Inventory
(NPI)-agitation/aggression subscore of ≥4.
- No response or suboptimal response to standard nonpharmacological interventions.
Exclusion Criteria:
- The agitation/aggression is attributable to concomitant medications, environmental
conditions, or active medical or psychiatric condition.
- Current diagnosis of major depressive disorder according to the criteria of the
Diagnostic and Statistical Manual of Mental Disorders Fourth Edition Text Revision
(DSM IV TR).
- Has persistent and distressing psychotic symptoms (delusion and/or hallucinations)
that require psychiatric hospitalization.
We found this trial at
58
sites
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