drugset / Trial / NCT00322153

A Study of the Safety and Efficacy of Memantine in Moderate to Severe Alzheimer's Disease

NCT00322153

Phase 3 Completed 677 enrolled Forest Laboratories
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study is to evaluate the safety, tolerability, and efficacy of memantine compared to placebo in outpatients diagnosed with moderate-to-severe dementia of the Alzheimer's type on a concurrent acetylcholinesterase inhibitor (AChEI).

Timeline

Start
2005-06
Primary completion
2007-10
Completion
2008-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Memantine Unknown 28 mg Oral

Indications