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

Outcome

Outcome not reported

Stopped: “The decision to stop the trial was based on efficacy results in the overall schizophrenia participant population.”

Drugs

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

Indications