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Completed Phase 2 Interventional Accepts healthy volunteers

Study Of GW679769 In Major Depressive Disorder

ClinicalTrials.gov ID: NCT00102492

Public ClinicalTrials.gov record NCT00102492. 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 5, 2026, 11:29 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 Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Fixed-Dose Study Evaluating the Efficacy and Safety of GW679769 in Subjects With Major Depressive Disorder.

Brief summary

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

This is a placebo-controlled, fixed dose study that will evaluate the efficacy and safety of GW679769 in subjects with major depressive disorder.

Study identification

NCT ID
NCT00102492
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
356 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 64 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Sep 30, 2004
Primary completion
Aug 31, 2006
Completion
Aug 31, 2006
Last update posted
Apr 15, 2015

2004 – 2006

United States locations

U.S. sites
27
U.S. states
17
U.S. cities
26
Facility City State ZIP Site status
GSK Investigational Site Scottsdale Arizona 85251
GSK Investigational Site Little Rock Arkansas 72223
GSK Investigational Site Beverly Hills California 90210
GSK Investigational Site Fort Lauderdale Florida 33301
GSK Investigational Site Miami Florida 33125
GSK Investigational Site North Miami Florida 33161
GSK Investigational Site Orlando Florida 32806
GSK Investigational Site Winter Park Florida 32789
GSK Investigational Site Marietta Georgia 30060
GSK Investigational Site Smyrna Georgia 30080
GSK Investigational Site Oakbrook Terrace Illinois 60181
GSK Investigational Site Shreveport Louisiana 71104
GSK Investigational Site Rockville Maryland 20852
GSK Investigational Site Farmington Hills Michigan 48336
GSK Investigational Site Saint Charles Missouri 63301
GSK Investigational Site Clementon New Jersey 08021
GSK Investigational Site Brooklyn New York 11235
GSK Investigational Site New York New York 10021
GSK Investigational Site New York New York 10024
GSK Investigational Site Beachwood Ohio 44122
GSK Investigational Site Eugene Oregon 97401
GSK Investigational Site Portland Oregon 97209
GSK Investigational Site Memphis Tennessee 38119
GSK Investigational Site Austin Texas 78756
GSK Investigational Site Irving Texas 75039
GSK Investigational Site Lake Jackson Texas 77566
GSK Investigational Site Bellevue Washington 98004

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00102492, 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 Apr 15, 2015 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00102492 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →