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Completed Phase 3 Interventional Results available

A Study In Patients With Type 2 Diabetes Mellitus

ClinicalTrials.gov ID: NCT00256867

Public ClinicalTrials.gov record NCT00256867. 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 Jul 24, 2026, 8:13 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 16 Week Randomized, Double-blind, Parallel Group Study to Evaluate the Efficacy and Safety of a New Medication (GSK523338) to Lower LDL-c and HbA1c in Subjects With Type 2 Diabetes Mellitus

Study identification

NCT ID
NCT00256867
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
369 participants

Conditions and interventions

Interventions

  • GSK523338 Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Aug 17, 2005
Primary completion
Oct 30, 2006
Completion
Oct 30, 2006
Last update posted
Jul 1, 2018

2005 – 2006

United States locations

U.S. sites
43
U.S. states
23
U.S. cities
41
Facility City State ZIP Site status
GSK Investigational Site Tucson Arizona 85745
GSK Investigational Site Fresno California 93720
GSK Investigational Site Wheat Ridge Colorado 80033
GSK Investigational Site Waterbury Connecticut 06708
GSK Investigational Site Miami Florida 33156
GSK Investigational Site Saint Cloud Florida 34769
GSK Investigational Site Atlanta Georgia 30308
GSK Investigational Site Chicago Illinois 60607
GSK Investigational Site Melrose Park Illinois 60160
GSK Investigational Site Springfield Illinois 62704
GSK Investigational Site Avon Indiana 46123
GSK Investigational Site Elkhart Indiana 46515
GSK Investigational Site Sunset Louisiana 70584
GSK Investigational Site Waltham Massachusetts 02453
GSK Investigational Site City of Saint Peters Missouri 63376
GSK Investigational Site Billings Montana 59102
GSK Investigational Site Las Vegas Nevada 89103
GSK Investigational Site Jamaica New York 11432
GSK Investigational Site Rochester New York 14609
GSK Investigational Site Columbus Ohio 43212
GSK Investigational Site Bend Oregon 97701
GSK Investigational Site Portland Oregon 97216
GSK Investigational Site Portland Oregon 97219
GSK Investigational Site Portland Oregon 97239
GSK Investigational Site Tualatin Oregon 97062
GSK Investigational Site Beaver Pennsylvania 15009
GSK Investigational Site Fleetwood Pennsylvania 19522
GSK Investigational Site Jefferson Hills Pennsylvania 15025
GSK Investigational Site Philadelphia Pennsylvania 19152
GSK Investigational Site Clinton South Carolina 29325
GSK Investigational Site Columbia South Carolina 29201
GSK Investigational Site Kingsport Tennessee 37660
GSK Investigational Site Bryan Texas 77802
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site Georgetown Texas 78626
GSK Investigational Site Midland Texas 79705
GSK Investigational Site Plano Texas 75093
GSK Investigational Site Salt Lake City Utah 84143
GSK Investigational Site Burke Virginia 22015
GSK Investigational Site Manassas Virginia 20110
GSK Investigational Site Bellevue Washington 98004
GSK Investigational Site Spokane Washington 99208
GSK Investigational Site Vancouver Washington 98664

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 42 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00256867, 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 Jul 1, 2018 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00256867 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →