drugset / Trial / NCT00301574

An Efficacy and Safety Study of Galantamine for the Treatment of Patients With Alzheimer's Disease.

NCT00301574

Phase 3 Completed 398 enrolled Janssen Pharmaceutical K.K.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of two fixed doses (16mg/day and 24mg/day) of galantamine (a drug for treating dementia) versus placebo for the treatment of patients with Alzheimer's disease, and to investigate the dose-response.

Timeline

Start
2001-04
Primary completion
Completion
2004-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Galantamine Small molecule 16 mg Oral
Subject Galantamine Small molecule 24 mg Oral

Indications