drugset / Trial / NCT00862992

Safety, Pharmacokinetics and Efficacy Study of MP-214 in Patients With Schizophrenia

NCT00862992

Phase 2 Completed 34 enrolled Tanabe Pharma Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety, pharmacokinetics and efficacy of 3 fixed doses of MP-214 orally administered once daily to patients with schizophrenia. MP-214 tablets will be administered to patients starting at an initial dose, followed by up-titration to a fixed dose (low, medium or high) for 14 days.

Timeline

Start
2008-04
Primary completion
2009-09
Completion
2009-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Cariprazine Small molecule 3 mg Oral
Subject Cariprazine Small molecule 6 mg Oral
Subject Cariprazine Small molecule 12.5 mg Oral

Indications