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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |