Study of the Efficacy and Safety of LY2940094 in Participants With Major Depressive Disorder (MDD)



Status:Completed
Conditions:Depression, Major Depression Disorder (MDD)
Therapuetic Areas:Psychiatry / Psychology, Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - 65
Updated:1/1/2014
Start Date:November 2012
End Date:March 2014
Contact:There may be multiple sites in this clinical trial 1-877-CTLILLY (1-877-285-4559) or
Phone:1-317-615-4559

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8-Week, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multi-center Study of the Efficacy and Safety of LY2940094 Administered Once Daily in Patients With Major Depressive Disorder (MDD)

This study will determine the efficacy, safety, and tolerability of a 40 mg once-daily (QD)
dose of LY2940094 for 8 weeks in participants with MDD.


Inclusion Criteria:

- Have a diagnosis of Major Depressive Disorder (MDD) without psychotic features as
defined in the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition,
Text Revision (DSM-IV-TR)

- Have clinically significant depressive symptoms defined by a GRID HAMD17 Total score
≥20 at screening

- Body mass index (BMI) between 18 and 35 kilogram per square meter (kg/m^2)

Exclusion Criteria:

- Have a current or previous diagnosis of bipolar I or II disorder, MDD with psychotic
features, schizoaffective disorder, schizophrenia, or other psychotic disorder

- Currently meeting the criteria of treatment-resistant depression defined as ≥2
documented, failed treatment trials of adequate dose and duration with a registered
antidepressant during the current depressive episode

- Had electroconvulsive treatment, transcranial magnetic stimulation, vagal nerve
stimulation for symptoms of depression in the 6 months prior to screening

- Have any clinically significant medical or uncontrolled condition or circumstance
prior to randomization that could affect participant safety
We found this trial at
10
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