drugset / Trial / NCT00216593

Treatment of Severe Alzheimer's Disease: Evaluation of Efficacy and Safety of Galantamine Hydrobromide in a Controlled Study

NCT00216593

Phase 3 Completed 415 enrolled Janssen Pharmaceutica N.V., Belgium
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the effectiveness and safety of galantamine hydrobromide treatment in patients with severe Alzheimer's disease.

Timeline

Start
2003-12
Primary completion
2007-09
Completion
2008-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Galantamine Small molecule 24 mg Oral

Indications