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Completed Phase 2 Interventional

An 8 Week Study Of Depression In Adults Diagnosed With Major Depressive Disorder

ClinicalTrials.gov ID: NCT00057213

Public ClinicalTrials.gov record NCT00057213. 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 22, 2026, 9:13 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 Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Flexible-Dose Study Evaluating Efficacy, Safety, and Tolerability of Once-Daily Oral GW353162 (20-40-60mg) Versus Placebo in Subjects With Major Depressive Disorder Over an Eight-Week Treatment Period.

Brief summary

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

A Placebo Controlled Study Evaluating Efficacy, Safety and Tolerability of Medication in Patients with Major Depressive Disorder (MDD)

Study identification

NCT ID
NCT00057213
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
367 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 64 Years
Sex
All
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
Feb 28, 2003
Primary completion
Mar 31, 2007
Completion
Mar 31, 2007
Last update posted
Apr 15, 2015

2003 – 2007

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
GSK Investigational Site Peoria Arizona 85381 - 4828
GSK Investigational Site Scottsdale Arizona 85251
GSK Investigational Site Garden Grove California 92845
GSK Investigational Site Irvine California 92618
GSK Investigational Site National City California 91950
GSK Investigational Site Miami Florida 33173
GSK Investigational Site Winter Park Florida 32789
GSK Investigational Site Springfield Illinois 62702
GSK Investigational Site Terre Haute Indiana 47802
GSK Investigational Site Florence Kentucky 41042
GSK Investigational Site Brockton Massachusetts 2301
GSK Investigational Site New York New York 10021
GSK Investigational Site Chapel Hill North Carolina 27514
GSK Investigational Site Raleigh North Carolina 27609
GSK Investigational Site Lyndhurst Ohio 44124
GSK Investigational Site Eugene Oregon 97401
GSK Investigational Site Philadelphia Pennsylvania 19106
GSK Investigational Site Austin Texas 78756
GSK Investigational Site Galveston Texas 77555
GSK Investigational Site Lake Jackson Texas 77566
GSK Investigational Site Salt Lake City Utah 84107

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 NCT00057213, 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 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00057213 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →