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A Study of the Effects of a New Antidepressant Treatment (GSK561679) in Females With Major Depressive Disorder - NCT00733980-53223(Clinical Trial 236001)



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City:  Brown Deer
State:  
WI
Zip Code: 53223
Conditions: Major Depressive Disorder (MDD)
Purpose: This six-week study will evaluate the efficacy, safety and tolerability of GSK561679 compared to placebo in female subjects with major depressive disorder
Study summary:
Criteria: Key Inclusion: Major depressive episode associated with Major Depressive Disorder (DSM-IV-TR criteria) - Duration of current episode is at least 4 weeks duration - Subjects who agree to use acceptable methods of birth control throughout the study Key Exclusion: - Subjects with a diagnosis or history of dementia, schizophrenia, bipolar disorder, borderline personality disorder, anorexia, bulimia, suicide attempts or suicidal behavior will not be eligible to participate. - Subjects who have significant lab abnormalities or unstable medical conditions - Subject has initiated psychotherapy within one month prior to the Screening visit - Received electroconvulsive therapy or transcranial magnetic stimulation within 6 months prior to screening - Failed to respond to an adequate course of pharmacotherapy of at least 2 different classes of antidepressants - Positive urine drug screen or positive blood alcohol - Pregnant or nursing - Received psychoactive drugs (except sleep aids) within 1 week of screening visit
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Data Source: ClinicalTrials.gov
Date Processed: April 13, 2010
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