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Completed Phase 3 Interventional

A Study of Taspoglutide Versus Placebo for the Treatment of Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Metformin Plus Pioglitazone.

ClinicalTrials.gov ID: NCT00744367

Public ClinicalTrials.gov record NCT00744367. 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 25, 2026, 12:01 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 Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Safety, Tolerability and Effect of Taspoglutide on Glycemic Control Compared to Placebo in Patients With Type II Diabetes Mellitus Inadequately Controlled With Metformin Plus Pioglitazone

Brief summary

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

This 3 arm study will assess the efficacy of taspoglutide on glycemic control (as assessed by HbA1c) in patients with type 2 diabetes mellitus inadequately controlled with metformin plus pioglitazone, compared to placebo after 24 weeks of treatment. Patients will be randomized to one of 3 treatment arms: taspoglutide 10mg once weekly, taspoglutide 20 mg once weekly (after 4 weeks of taspoglutide 10 mg once weekly) or placebo, in addition to their continued stable metformin plus pioglitazone treatment. After the first 24 weeks patients on placebo will be switched to taspoglutide 10mg once weekly or taspoglutide 20mg once weekly (after 4 weeks of taspoglutide 10mg once weekly. The anticipated time on study treatment is 1-2 years, and the target sample size is 100-500 individuals.

Study identification

NCT ID
NCT00744367
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
326 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
Oct 2008 (Type not available)
Primary completion
Nov 2010 (Actual)
Completion
Nov 2010 (Actual)
Last update posted
Aug 5, 2016

2008 – 2010

United States locations

U.S. sites
76
U.S. states
32
U.S. cities
71
Facility City State ZIP Site status
Not listed Birmingham Alabama 35209 —
Not listed Birmingham Alabama 35294 —
Not listed Huntsville Alabama 35801 —
Not listed Muscle Shoals Alabama 35661 —
Not listed Phoenix Arizona 85028 —
Not listed Phoenix Arizona 85032 —
Not listed Buena Park California 90620 —
Not listed Lancaster California 93534 —
Not listed Loma Linda California 92354 —
Not listed Rancho Cucamonga California 91730 —
Not listed Roseville California 95661 —
Not listed San Diego California 92161 —
Not listed Walnut Creek California 94598 —
Not listed Wheat Ridge Colorado 80033 —
Not listed Hamden Connecticut 06518 —
Not listed Washington D.C. District of Columbia 20017 —
Not listed Bradenton Florida 34208 —
Not listed Chiefland Florida 32626 —
Not listed Fort Myers Florida 33907 —
Not listed Gainesville Florida 32607 —
Not listed Hollywood Florida 33021 —
Not listed Miami Florida 33136 —
Not listed New Port Richey Florida 34652 —
Not listed Ocala Florida 34474 —
Not listed Plantation Florida 33317 —
Not listed Tampa Florida 33614 —
Not listed Nampa Idaho 83687 —
Not listed Aurora Illinois 60504 —
Not listed Libertyville Illinois 60048 —
Not listed Evansville Indiana 47714 —
Not listed Des Moines Iowa 50314 —
Not listed Topeka Kansas 66614 —
Not listed Lexington Kentucky 40504 —
Not listed Madisonville Kentucky 42431 —
Not listed New Orleans Louisiana 70121 —
Not listed Frederick Maryland 21702 —
Not listed Oxon Hill Maryland 20745 —
Not listed Detroit Michigan 48202 —
Not listed Ferndale Michigan 48220 —
Not listed Kalamazoo Michigan 49048 —
Not listed Biloxi Mississippi 39531 —
Not listed Olive Branch Mississippi 38654 —
Not listed City of Saint Peters Missouri 63376 —
Not listed Omaha Nebraska 68114 —
Not listed Omaha Nebraska 68131 —
Not listed Las Vegas Nevada 89148 —
Not listed Albany New York 12206-1098 —
Not listed Brooklyn New York 11218 —
Not listed Hudson New York 12534 —
Not listed Lake Success New York 11042 —
Not listed Staten Island New York 10301 —
Not listed Charlotte North Carolina 28262 —
Not listed Charlotte North Carolina 28277 —
Not listed Mooresville North Carolina 28117 —
Not listed Wilmington North Carolina 28401 —
Not listed Bismarck North Dakota 58501 —
Not listed Athens Ohio 45701 —
Not listed Cincinnati Ohio 45219 —
Not listed Kettering Ohio 45429 —
Not listed Norman Oklahoma 73071 —
Not listed Medford Oregon 97504 —
Not listed Beaver Pennsylvania 15009 —
Not listed Bensalem Pennsylvania 19020 —
Not listed Carlisle Pennsylvania 17015 —
Not listed Levittown Pennsylvania 19056 —
Not listed Melrose Park Pennsylvania 19027 —
Not listed Pittsburgh Pennsylvania 15236 —
Not listed Cranston Rhode Island 02920 —
Not listed Greer South Carolina 29651 —
Not listed Bellaire Texas 77401 —
Not listed Dallas Texas 75230 —
Not listed Dallas Texas 75231 —
Not listed Houston Texas 77030 —
Not listed San Antonio Texas 78205 —
Not listed Salt Lake City Utah 84102 —
Not listed Federal Way Washington 98003 —

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 37 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00744367, 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 Aug 5, 2016 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00744367 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →