drugset / Trial / NCT01086748

A Study in Schizophrenia Patients

NCT01086748

Phase 2 Completed 880 enrolled Eli Lilly and Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

An inpatient/outpatient study to see if LY2140023 is better than placebo in acutely ill patients with schizophrenia.

Timeline

Start
2010-03
Primary completion
2012-05
Completion
2012-05

Drugs

EvaluationDrugModalityDoseRoute
Subject LY2140023 Unknown 40 mg Oral
Subject LY2140023 Unknown 80 mg Oral
Comparator Risperidone Other / unclassified 2 mg Oral

Indications