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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT00057239

Public ClinicalTrials.gov record NCT00057239. 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 Nov 7, 2026, 12:47 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Fixed-Dose Study Evaluating the Efficacy, Safety and Tolerability of Two Doses (20mg and 60mg) of a Once-Daily Oral Formulation of GW353162 in Subjects With Major Depressive Disorder for a Treatment Period of Eight Weeks

Brief summary

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

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

Study identification

NCT ID
NCT00057239
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
546 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
Mar 2003 (Type not available)
Primary completion
May 2004 (Actual)
Completion
May 2004 (Actual)
Last update posted
Oct 4, 2010

2003 – 2004

United States locations

U.S. sites
29
U.S. states
19
U.S. cities
28
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72223 —
GSK Investigational Site Newport Beach California 92660-2814 —
GSK Investigational Site Farmington Connecticut 6708 —
GSK Investigational Site Largo Florida 33773 —
GSK Investigational Site Maitland Florida 32751 —
GSK Investigational Site Miami Florida 33156 —
GSK Investigational Site North Miami Florida 33161 —
GSK Investigational Site Edwardsville Illinois 62025 —
GSK Investigational Site Glen Burnie Maryland 21061 —
GSK Investigational Site Farmington Hills Michigan 48336 —
GSK Investigational Site Minneapolis Minnesota 55454 —
GSK Investigational Site Clementon New Jersey 08021 —
GSK Investigational Site Kenilworth New Jersey 07033 —
GSK Investigational Site Lawrence New York 11559 —
GSK Investigational Site Charlotte North Carolina 28203 —
GSK Investigational Site Cleveland Ohio 44106 —
GSK Investigational Site Dayton Ohio 45408 —
GSK Investigational Site Oklahoma City Oklahoma 73118 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Portland Oregon 97209 —
GSK Investigational Site Portland Oregon 97210 —
GSK Investigational Site Conshohocken Pennsylvania 19428 —
GSK Investigational Site Dallas Texas 75235 —
GSK Investigational Site Houston Texas 77004 —
GSK Investigational Site Irving Texas 75039 —
GSK Investigational Site Woodstock Vermont 05091 —
GSK Investigational Site Seattle Washington 98104 —
GSK Investigational Site Tacoma Washington 98499 —
GSK Investigational Site Brown Deer Wisconsin 53223 —

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 NCT00057239, 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 Oct 4, 2010 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00057239 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →