Clinical Trial Details


Research Study Summary

A 17-week, Phase 2, Multicenter, Randomized, Double-Blind Study of Treatment with LY2140023 Combined with SOC to placebo Combined with SOC as the Treatment of Patients with DSM-IV-TR Schizophrenia with Prominent Negative Symptoms


The primary objective of this study is to determine if treatment with LY2140023 compared to placebo (an inactive substance), when added to a fixed dose of a standard of care (SOC) antipsychotic, will demonstrate significantly greater reduction of negative symptoms.

Patients included in this study will be concurrently receiving 1 of 4 current FDA approved antipsychotics: aripiprazole, olanzapine, risperidone, or quetiapine

Please contact Alexian Brothers for more information on participation.

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CW ID: 176871
Date Last Changed: July 22, 2013

Clinical Trial Snapshot

Both Male and Female
Overall Status
17 Weeks
Facility Type


Alexian Brothers Hospital Network
1786 Moon Lake Boulevard, Suite 200
Hoffman Estates, IL 60169
Phone: 847-230-3599

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Research Center Information:

Alexian Brothers Hospital Network

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