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Completed Phase 3 Interventional

Efficacy and Safety Study of Rosiglitazone/Metformin Therapy vs Rosiglitazone and Metformin in Type 2 Diabetes Subjects

ClinicalTrials.gov ID: NCT00499707

Public ClinicalTrials.gov record NCT00499707. 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 17, 2026, 8:44 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 Randomized, Double-blind Trial to Evaluate the Efficacy and Safety of Fixed Dose Rosiglitazone/Metformin Combination Therapy Compared to Both Rosiglitazone and Metformin Monotherapies in Drug Naive Type 2 Diabetes Mellitus Subjects

Brief summary

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

The purpose of this 32 week study is to demonstrate that fixed-dose combination treatment with rosiglitazone/metformin will safely and effectively control glycemia as first line oral therapy in subjects type 2 diabetes. The primary objective of the study is to demonstrate superiority of rosiglitazone/metformin compared to its rosiglitazone and metformin.

Study identification

NCT ID
NCT00499707
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
453 participants

Conditions and interventions

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
Oct 8, 2003 (Type not available)
Primary completion
Dec 1, 2004 (Actual)
Completion
Dec 16, 2004 (Actual)
Last update posted
Mar 21, 2018

2003 – 2004

United States locations

U.S. sites
48
U.S. states
18
U.S. cities
44
Facility City State ZIP Site status
GSK Investigational Site Anniston Alabama 36207 —
GSK Investigational Site Chandler Arizona 85224 —
GSK Investigational Site Phoenix Arizona 85014 —
GSK Investigational Site Phoenix Arizona 85050 —
GSK Investigational Site Tucson Arizona 85745 —
GSK Investigational Site Encinitas California 92024 —
GSK Investigational Site Fullerton California 92835 —
GSK Investigational Site Los Banos California 93635 —
GSK Investigational Site Mission Viejo California 92691 —
GSK Investigational Site Jacksonville Florida 32204 —
GSK Investigational Site Melbourne Florida 32901 —
GSK Investigational Site Miami Florida 33156 —
GSK Investigational Site Orlando Florida 32806 —
GSK Investigational Site Saint Cloud Florida 34769 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Fayetteville Georgia 30214 —
GSK Investigational Site Woodstock Georgia 30189 —
GSK Investigational Site Chicago Illinois 60607 —
GSK Investigational Site Evansville Indiana 47713 —
GSK Investigational Site Newburgh Indiana 47630 —
GSK Investigational Site Slidell Louisiana 70461 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site Chesterfield Missouri 63017 —
GSK Investigational Site Kansas City Missouri 64111 —
GSK Investigational Site St Louis Missouri 63376 —
GSK Investigational Site Las Vegas Nevada 89103 —
GSK Investigational Site Kingston New York 12401 —
GSK Investigational Site New York New York 10024 —
GSK Investigational Site New York New York 10029 —
GSK Investigational Site New York New York 10032 —
GSK Investigational Site Rochester New York 14609 —
GSK Investigational Site Charlotte North Carolina 28210 —
GSK Investigational Site Mogadore Ohio 44260 —
GSK Investigational Site Downingtown Pennsylvania 19335 —
GSK Investigational Site Warminster Pennsylvania 18974 —
GSK Investigational Site West Chester Pennsylvania 19382 —
GSK Investigational Site Bristol Tennessee 37620 —
GSK Investigational Site Johnson City Tennessee 37601 —
GSK Investigational Site Arlington Texas 76017 —
GSK Investigational Site Beaumont Texas 77701 —
GSK Investigational Site Bryan Texas 77802 —
GSK Investigational Site Dallas Texas 75230 —
GSK Investigational Site Midland Texas 79705 —
GSK Investigational Site San Antonio Texas 78221 —
GSK Investigational Site San Antonio Texas 78237 —
GSK Investigational Site Seattle Washington 98108 —
GSK Investigational Site Spokane Washington 99207 —
GSK Investigational Site Wenatchee Washington 98801 —

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 54 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00499707, 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 Mar 21, 2018 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00499707 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →