drugset / Trial / NCT01307800

A Study of LY2140023 in Patients With Schizophrenia

NCT01307800 ↗

Phase 3 Terminated 567 enrolled Denovo Biopharma LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine whether at least 1 dose level of LY2140023 given to acutely ill patients with schizophrenia will demonstrate significantly greater efficacy as compared to placebo.

Timeline

Start
2011-03
Primary completion
2012-09
Completion
2012-09

Outcome

Missed primary endpoint

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

registry 80 mg LY2140023, BID vs Placebo; p = 0.994; LS mean difference 4.1 (95% CI -0.5 to 8.8) NCT01307800 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject LY2140023 Unknown 10 mg Oral
Subject LY2140023 Unknown 40 mg Oral
Subject LY2140023 Unknown 80 mg Oral

Indications