drugset / Trial / NCT00254202

Efficacy and Safety of Iloperidone Compared With Placebo and Active Control in Subjects With Acute Schizophrenia

NCT00254202

Phase 3 Completed 593 enrolled Vanda Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the safety and efficacy of iloperidone compared to placebo and an active comparator in the treatment of patients with schizophrenia in acute exacerbation.

Timeline

Start
2005-11-18
Primary completion
2006-09-26
Completion
2007-03-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Iloperidone Small molecule Oral
Comparator Ziprasidone Small molecule Oral

Indications