drugset / Trial / NCT00645190

A Randomized, Double-blind, Flexible Dose, Multicenter Study to Evaluate the Effectiveness and Safety of Galantamine IR in Mild to Moderate Alzheimer's Disease

NCT00645190

Phase 3 Completed 215 enrolled Xian-Janssen Pharmaceutical Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this randomized, double-blind, active-controlled, flexible dosage, multicenter study is to evaluate the effectiveness and safety of galantamine tablet (16-24mg/day) for 16 weeks in the treatment of mild to moderate Alzheimer's Disease (AD) comparing with Donepezil.

Timeline

Start
2004-03
Primary completion
Completion
2005-02

Drugs

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

Indications