drugset / Trial / NCT01125358

A Study in Schizophrenic Patients

NCT01125358

Phase 2 Terminated 82 enrolled Denovo Biopharma LLC
RandomizedParallel-groupTriple-blindTreatment

Summary

This study is designed to compare 3 doses of LY2140023 for the treatment of schizophrenia as assessed at endpoint (up to 7 weeks) using the Clinical Utility Index (CUI), a measure of efficacy, safety, and tolerability.

Timeline

Start
2010-05
Primary completion
2012-09
Completion
2012-09

Drugs

EvaluationDrugModalityDoseRoute
Subject LY2140023 Unknown 10 mg Oral
Subject LY2140023 Unknown 80 mg Oral
Subject LY2140023 Unknown 160 mg Oral

Indications