drugset / Trial / NCT00810147

A Phase II, Multicenter, Double Blind, Placebo-Controlled Safety, Tolerability Study of BMS-708163 in Patients With Mild to Moderate Alzheimer's Disease

NCT00810147

Phase 2 Completed 209 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the safety and tolerability of BMS-708163 in patients with mild to moderate Alzheimer's disease over a treatment period of 12-weeks and the course of any potential effects during a 12-week wash-out period

Timeline

Start
2009-02
Primary completion
2010-06
Completion
2010-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Avagacestat Small molecule 25 mg Oral
Comparator Avagacestat Small molecule 50 mg Oral
Comparator Avagacestat Small molecule 100 mg Oral
Comparator Avagacestat Small molecule 125 mg Oral

Indications