Overview

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

Status:
Completed
Trial end date:
2008-09-01
Target enrollment:
0
Participant gender:
All
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.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sunovion
Criteria
Inclusion Criteria:

- Mild to moderate Alzheimer's Disease

- Male or female 55 years or older

- Living with caregiver

- Read, understand and speak English

Exclusion Criteria:

- Need to drive during the study

- Treatment with acetylcholinesterase inhibitors or NMDA antagonist, such as Aricept or
Namenda, within 2 weeks of check-up and during the study

- Frequent Smoker

- Frequent Consumer of Caffeine