Study Of GW679769 In Major Depressive Disorder
Status: | Completed |
---|---|
Conditions: | Depression, Depression, Major Depression Disorder (MDD) |
Therapuetic Areas: | Psychiatry / Psychology, Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 18 - 64 |
Updated: | 10/14/2017 |
Start Date: | October 2004 |
End Date: | September 2006 |
A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Fixed-Dose Study Evaluating the Efficacy and Safety of GW679769 in Subjects With Major Depressive Disorder.
This is a placebo-controlled, fixed dose study that will evaluate the efficacy and safety of
GW679769 in subjects with major depressive disorder.
GW679769 in subjects with major depressive disorder.
Inclusion criteria:
- Subjects must have the ability to comprehend the key components of the consent form.
- Subject must have met DSM-IV-TR (Diagnostic and Statistical Manual of Mental
Disorders, Fourth Edition, Text Revision) criteria for current MDE (major depressive
episode) for at least 8 weeks prior to the Screening Visit.
- If female, subjects must be practicing an acceptable method of birth control.
- Subjects must have rating scores as outlined.
Exclusion criteria:
- Subjects whose symptoms of the MDE are better accounted for by another diagnosis.
- Subjects with a history of schizophrenia, schizoaffective disorders or bipolar
disorder.
- Subjects have a positive urine test for illicit drug use and/or a history of substance
abuse or alcohol dependence within the past 12 months.
- Subjects with an unstable medical disorder.
- If female, pregnant or lactating.
- Subjects who have received ECT (electroconvulsive therapy) or TMS (transcranial
magnetic stimulation) within the 6 months preceding screening or who have ever been
homicidal.
We found this trial at
27
sites
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