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Completed Phase 2 Interventional Results available

A Study of the Effects of a New Antidepressant Treatment (GSK561679) in Females With Major Depressive Disorder

ClinicalTrials.gov ID: NCT00733980

Public ClinicalTrials.gov record NCT00733980. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 7, 2026, 12:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Six-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Evaluating the Efficacy, Safety, and Tolerability of GSK561679 Compared to Placebo in Female Subjects, Diagnosed With Major Depressive Disorder

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This six-week study will evaluate the efficacy, safety and tolerability of GSK561679 compared to placebo in female subjects with major depressive disorder

Study identification

NCT ID
NCT00733980
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 64 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 1, 2008
Primary completion
Jun 17, 2010
Completion
Jun 17, 2010
Last update posted
Nov 16, 2017

2008 – 2010

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
GSK Investigational Site Cerritos California 90703
GSK Investigational Site San Diego California 92108
GSK Investigational Site Torrance California 90502
GSK Investigational Site Jacksonville Florida 32216
GSK Investigational Site Miami Florida 33125
GSK Investigational Site Atlanta Georgia 30322
GSK Investigational Site Marietta Georgia 30060
GSK Investigational Site Chicago Illinois 60612
GSK Investigational Site Skokie Illinois 60076
GSK Investigational Site Shreveport Louisiana 71104
GSK Investigational Site Rockville Maryland 20852
GSK Investigational Site Albuquerque New Mexico 87109
GSK Investigational Site Raleigh North Carolina 27609
GSK Investigational Site Cincinnati Ohio 45219-0516
GSK Investigational Site Philadelphia Pennsylvania 19104
GSK Investigational Site Memphis Tennessee 38119
GSK Investigational Site Brown Deer Wisconsin 53223
GSK Investigational Site Madison Wisconsin 53719

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00733980, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 16, 2017 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00733980 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →