drugset / Trial / NCT00658645

Efficacy of Bifeprunox in Patients With Schizophrenia

NCT00658645

Phase 3 Terminated 227 enrolled H. Lundbeck A/S
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of the study is to evaluate the efficacy of bifeprunox in the maintenance phase of schizophrenia compared to placebo.

Timeline

Start
2008-03
Primary completion
2009-08
Completion
2009-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Bifeprunox Small molecule 20 mg Oral
Comparator Quetiapine Small molecule 600 mg Oral

Indications