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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 Oct 27, 2026, 12:28 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

Brief summary

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

This study evaluates the effect of medicines for type 2 diabetes and lipids control. This study will require about 6 office visits for lab tests and examinations. All study related medicines and medical examinations will be provided at no cost to the subjects.

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

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 18, 2005 (Actual)
Primary completion
Oct 31, 2006 (Actual)
Completion
Oct 31, 2006 (Actual)
Last update posted
Jul 2, 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 2, 2018 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00256867 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →