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Completed Phase 2 Interventional Results available

A New Oral Treatment For Type II Diabetes Mellitus

ClinicalTrials.gov ID: NCT00111800

Public ClinicalTrials.gov record NCT00111800. 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 Sep 3, 2026, 9:50 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 12-Week, Parallel-Group, Double-Blind, Randomized, Placebo-Controlled, Multicenter, Dose Ranging Study to Evaluate the Efficacy, Safety and Tolerability of Denagliptin, Administered Orally, Once Daily, as Monotherapy in Subjects With Type 2 Diabetes Mellitus Followed by a 12-week Active Treatment Extension

Brief summary

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

This is a 24-week study investigating the safety and efficacy of several dosages of a potential new oral medicine for Type II diabetes mellitus.

Study identification

NCT ID
NCT00111800
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
375 participants

Conditions and interventions

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
Apr 27, 2005
Primary completion
Jun 30, 2006
Completion
Jul 20, 2006
Last update posted
Mar 20, 2018

2005 – 2006

United States locations

U.S. sites
36
U.S. states
20
U.S. cities
35
Facility City State ZIP Site status
GSK Investigational Site Long Beach California 90806
GSK Investigational Site Pasadena California 91105
GSK Investigational Site Denver Colorado 80220
GSK Investigational Site Hollywood Florida 33021
GSK Investigational Site Miami Florida 33126
GSK Investigational Site Atlanta Georgia 30308
GSK Investigational Site Marietta Georgia 30066
GSK Investigational Site Honolulu Hawaii 96813
GSK Investigational Site Chicago Illinois 60607
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site Sunset Louisiana 70584
GSK Investigational Site Oxon Hill Maryland 20745
GSK Investigational Site Las Vegas Nevada 89106
GSK Investigational Site Pahrump Nevada 89048
GSK Investigational Site Albany New York 12208
GSK Investigational Site Buffalo New York 14209
GSK Investigational Site Johnson City New York 13790
GSK Investigational Site Rochester New York 14642
GSK Investigational Site Syracuse New York 13210
GSK Investigational Site Durham North Carolina 27710
GSK Investigational Site Raleigh North Carolina 27612
GSK Investigational Site Cincinnati Ohio 45246
GSK Investigational Site Kettering Ohio 45429
GSK Investigational Site Jefferson Hills Pennsylvania 15025
GSK Investigational Site Sewickley Pennsylvania 15143
GSK Investigational Site Columbia South Carolina 29201
GSK Investigational Site Kingsport Tennessee 37660
GSK Investigational Site Arlington Texas 76017
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site Dallas Texas 75246
GSK Investigational Site San Antonio Texas 78237
GSK Investigational Site Salt Lake City Utah 84102
GSK Investigational Site Burke Virginia 22015
GSK Investigational Site Bellingham Washington 98226
GSK Investigational Site Tacoma Washington 98403
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 73 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00111800, 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 20, 2018 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00111800 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →