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ClinicalTrials.gov record
Completed Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT00754988

Public ClinicalTrials.gov record NCT00754988. 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 2, 2026, 9:45 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-dummy, Placebo and Active-controlled Study to Assess the Safety, Tolerability and Effect of Taspoglutide on Glycemic Control Compared to Sitagliptin and Placebo in Patients With Type II Diabetes Mellitus Inadequately Controlled With Metformin.

Brief summary

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

This 4 arm study will assess the efficacy, safety and tolerability of taspoglutide compared to sitagliptin and placebo in patients with type 2 diabetes mellitus inadequately controlled with metformin. Patients will be randomized to receive taspoglutide (10mg once weekly or 10mg once weekly for 4 weeks followed by 20mg once weekly), sitagliptin 100mg once daily or placebo, in a ratio of 2:2:2:1, in addition to their continued prestudy metformin treatment. After 24 weeks of treatment, patients on active treatment will continue on the same treatment and 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 2+ years, and the target sample size is 500+ individuals.

Study identification

NCT ID
NCT00754988
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
666 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
Sep 30, 2008
Primary completion
Feb 28, 2011
Completion
Feb 28, 2011
Last update posted
Nov 3, 2016

2008 – 2011

United States locations

U.S. sites
64
U.S. states
27
U.S. cities
61
Facility City State ZIP Site status
Not listed Birmingham Alabama 35233
Not listed Huntsville Alabama 35802
Not listed Tallassee Alabama 36078
Not listed Scottsdale Arizona 85254
Not listed Little Rock Arkansas 72205
Not listed Huntington Beach California 92646
Not listed La Jolla California 92037
Not listed Los Angeles California 90017
Not listed Roseville California 95661
Not listed San Francisco California 94109
Not listed Tacoma California 98405
Not listed Colorado Springs Colorado 80904
Not listed New London Connecticut 06320
Not listed Manati District of Columbia 00674
Not listed Daytona Beach Florida 32117
Not listed Hialeah Florida 33012
Not listed Jacksonville Florida 32205
Not listed Miami Florida 33186
Not listed Panama City Florida 32401
Not listed Tampa Florida 33606
Not listed Augusta Georgia 30904
Not listed Conyers Georgia 30094
Not listed Snellville Georgia 30029
Not listed Honolulu Hawaii 96813
Not listed Indianapolis Indiana 46229
Not listed Indianapolis Indiana 46254
Not listed Lafayette Indiana 47905
Not listed South Bend Indiana 46628
Not listed Baltimore Maryland 21229
Not listed Brockton Massachusetts 02301
Not listed Cadillac Michigan 49601
Not listed Brooklyn Center Minnesota 55430
Not listed Minneapolis Minnesota 55416
Not listed City of Saint Peters Missouri 63376
Not listed Fulton New York 13069
Not listed Hudson New York 12534
Not listed Rochester New York 14609
Not listed Charlotte North Carolina 28211
Not listed Raleigh North Carolina 27609
Not listed Shelby North Carolina 28150
Not listed Statesville North Carolina 28625
Not listed Winston-Salem North Carolina 27103
Not listed Columbus Ohio 43213
Not listed Delaware Ohio 43015
Not listed Marion Ohio 43302
Not listed Corvallis Oregon 97330
Not listed Eugene Oregon 97401
Not listed Aliquippa Pennsylvania 15001
Not listed Beaver Pennsylvania 15009
Not listed Erie Pennsylvania 16508
Not listed Reading Pennsylvania 17601
Not listed Reading Pennsylvania 19606
Not listed Shippensburg Pennsylvania 17257
Not listed Warminster Pennsylvania 18974
Not listed Anderson South Carolina 29621
Not listed Kingsport Tennessee 37660
Not listed Dallas Texas 75230
Not listed Houston Texas 77030
Not listed South Burlington Vermont 05403
Not listed Hampton Virginia 23666
Not listed Norfolk Virginia 23502
Not listed Richmond Virginia 23249
Not listed Richmond Virginia 23294
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 84 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00754988, 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 Nov 3, 2016 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00754988 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →