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Completed Phase 2 Interventional Results available

Dose-Ranging Study in Treatment Naive Type 2 Diabetes Mellitus(T2DM)

ClinicalTrials.gov ID: NCT00500331

Public ClinicalTrials.gov record NCT00500331. 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, 9:22 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 Double-blind, Randomized 12-week Study to Evaluate the Safety and Efficacy of GSK189075 Tablets vs Pioglitazone in Treatment Naive Subjects With Type 2 Diabetes Mellitus

Study identification

NCT ID
NCT00500331
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
334 participants

Conditions and interventions

Interventions

  • GSK189075 Drug
  • pioglitazone Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 70 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
Jan 22, 2007
Primary completion
Feb 13, 2008
Completion
Feb 13, 2008
Last update posted
Dec 5, 2017

2007 – 2008

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
GSK Investigational Site Mesa Arizona 85206
GSK Investigational Site Hollywood Florida 33023
GSK Investigational Site Miami Florida 33156
GSK Investigational Site Saint Cloud Florida 34769
GSK Investigational Site Sunset Louisiana 70584
GSK Investigational Site Oxon Hill Maryland 20745
GSK Investigational Site Las Vegas Nevada 89016
GSK Investigational Site Las Vegas Nevada 89106
GSK Investigational Site Las Vegas Nevada 89128
GSK Investigational Site Albuquerque New Mexico 87102
GSK Investigational Site Canal Fulton Ohio 44614
GSK Investigational Site Simpsonville South Carolina 29681
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site Burke Virginia 22015

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 122 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00500331, 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 Dec 5, 2017 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00500331 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →