drugset / Trial / NCT00285077

Long-Term Safety Extension With SR57667B in Patients With Alzheimer's Disease

NCT00285077 ↗

Phase 2 Completed 390 enrolled Sanofi
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective is to assess the long term safety/tolerability of 4 mg/day of SR57667B in comparison to placebo in patients with mild-to-moderate Alzheimer's Disease (AD). A secondary objective is to describe the long term progression of Alzheimer's symptoms in patients treated by 4 mg/day of SR57667B.

Timeline

Start
2004-03
Primary completion
2006-11
Completion
2006-11

Drugs

EvaluationDrugModalityDoseRoute
Subject SR57667B Unknown 4 mg —

Indications