drugset / Trial / NCT00905307

Study to Evaluate the Efficacy, Safety, and Tolerability of Oral OPC-34712 and Aripiprazole for Treatment of Acute Schizophrenia

NCT00905307 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

This will be a multicenter, randomized, double-blind, placebo-controlled study designed to assess the tolerability, safety, and efficacy of OPC-34712 (0.25 to 6.0 mg) for the treatment of adult subjects hospitalized with an acute relapse of schizophrenia. Aripiprazole (10 to 20 mg) is included as a positive control to confirm the assay sensitivity of the study. A total of approximately 563 subjects will be screened at an estimated 75 sites worldwide in order to obtain approximately 450 randomized subjects.

Timeline

Start
2009-07
Primary completion
2010-09
Completion
2010-11

Outcome

Missed primary endpoint

registry OPC-34712 Low-dose vs Placebo; p = 0.2846; Treatment difference -4.70 (95% CI -10.2 to 0.82); ANCOVA NCT00905307 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Aripiprazole Other / unclassified 10 mg Oral
Comparator Aripiprazole Other / unclassified 20 mg Oral
Subject Brexpiprazole Small molecule 0.25 mg —
Subject Brexpiprazole Small molecule 6 mg —

Indications