drugset / Trial / NCT00359944

Safety and Efficacy Study of AC-3933 in Adults With Mild to Moderate Alzheimer's Disease

NCT00359944 ↗

Phase 2 Completed 171 enrolled Sumitomo Pharma America, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to investigate efficacy and safety of different doses of AC-3933 in patients with mild to moderate Alzheimer's Disease.

Timeline

Start
2006-02
Primary completion
2008-09
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Subject RESEQUINIL Small molecule 5 mg —
Subject RESEQUINIL Small molecule 20 mg —

Indications