drugset / Trial / NCT00366327

Study Evaluating Bifeprunox in Patients With Schizophrenia.

NCT00366327

Phase 3 Terminated 400 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

An open-label extension study using a variable dose (20 to 30 mg daily) of bifeprunox to evaluate long-term safety.

Timeline

Start
2007-01
Primary completion
2008-03
Completion
2008-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Bifeprunox Small molecule 20 mg
Subject Bifeprunox Small molecule 30 mg

Indications