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Completed Phase 4 Interventional Results available

Efficacy and Safety of Toujeo® Versus Tresiba® in Insulin-Naive Patients With Type 2 Diabetes Mellitus Inadequately Controlled With Oral Antihyperglycemic Drug(s) ± GLP-1 Receptor Agonist

ClinicalTrials.gov ID: NCT02738151

Public ClinicalTrials.gov record NCT02738151. 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 21, 2026, 11:21 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 24-week, Multicenter, Randomized, Open-Label, Parallel-group StudyComparing the Efficacy and Safety of Toujeo® and Tresiba® in Insulin-NaivePatients With Type 2 Diabetes Mellitus Not Adequately Controlled With OralAntihyperglycemic Drug(s) ± GLP-1 Receptor Agonist

Brief summary

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

Primary Objective: To demonstrate the noninferiority in the efficacy of Toujeo® to Tresiba® in glycated hemoglobin (HbA1c) change from Baseline to Week 24. Secondary Objectives: Change From Baseline in HbA1c to Week 12 To assess the effects of the insulin Toujeo® in comparison with insulin Tresiba® at week 12 and week 24 on: * Change in Fasting plasma glucose (FPG); * Change in Fasting self-monitored plasma glucose (SMPG) and 4-point SMPG and 8-point SMPG profile; * Percentage of participants reaching HbA1c targets \<7% or ≤6.5%; * Percentage of participants reaching HbA1c targets \<7% or ≤6.5% without severe and/or confirmed hypoglycemia * Frequency of occurrence and diurnal distribution of hypoglycemia by American Diabetes Association (ADA) category of hypoglycemia. To assess the safety in each treatment group. To assess the treatment effects in each treatment group on Patient Reported Outcomes (PRO). Percentage of participants requiring rescue therapy.

Study identification

NCT ID
NCT02738151
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Sanofi
Industry
Enrollment
929 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
May 19, 2016 (Type not available)
Primary completion
Aug 15, 2017 (Actual)
Completion
Aug 15, 2017 (Actual)
Last update posted
Sep 14, 2018

2016 – 2017

United States locations

U.S. sites
74
U.S. states
24
U.S. cities
65
Facility City State ZIP Site status
Investigational Site Number 840038 Sheffield Alabama 35660 —
Investigational Site Number 840066 Phoenix Arizona 85020 —
Investigational Site Number 840051 Anaheim California 92801 —
Investigational Site Number 840081 Chino California 91710 —
Investigational Site Number 840016 Huntington Park California 90255 —
Investigational Site Number 840002 La Jolla California 92037 —
Investigational Site Number 840091 Los Angeles California 90017 —
Investigational Site Number 840058 Northridge California 91324 —
Investigational Site Number 840021 Palm Springs California 92262 —
Investigational Site Number 840087 Santa Ana California 92704 —
Investigational Site Number 840030 Torrance California 90505 —
Investigational Site Number 840065 Van Nuys California 91405 —
Investigational Site Number 840075 Bradenton Florida 34201 —
Investigational Site Number 840076 New Port Richey Florida 34652 —
Investigational Site Number 840026 Ocoee Florida 34761 —
Investigational Site Number 840052 Palm Harbor Florida 34684 —
Investigational Site Number 840080 Palm Harbor Florida 34684 —
Investigational Site Number 840018 Port Charlotte Florida 33952 —
Investigational Site Number 840071 Lawrenceville Georgia 30046 —
Investigational Site Number 840085 Roswell Georgia 30076 —
Investigational Site Number 840072 Statesboro Georgia 30461 —
Investigational Site Number 840039 Stockbridge Georgia 30281 —
Investigational Site Number 840036 Arlington Heights Illinois 60005 —
Investigational Site Number 840010 Chicago Illinois 60616 —
Investigational Site Number 840005 Avon Indiana 46123 —
Investigational Site Number 840063 Council Bluffs Iowa 51501 —
Investigational Site Number 840098 Des Moines Iowa 50134 —
Investigational Site Number 840101 Des Moines Iowa 50314 —
Investigational Site Number 840096 West Des Moines Iowa 50266 —
Investigational Site Number 840061 Paris Kentucky 40361 —
Investigational Site Number 840011 Hyattsville Maryland 20782 —
Investigational Site Number 840001 Rockville Maryland 20852 —
Investigational Site Number 840041 Flint Michigan 48504 —
Investigational Site Number 840057 Flint Michigan 48532 —
Investigational Site Number 840033 Troy Michigan 48085 —
Investigational Site Number 840084 Olive Branch Mississippi 38654 —
Investigational Site Number 840048 Chesterfield Missouri 63017 —
Investigational Site Number 840023 Las Vegas Nevada 89117 —
Investigational Site Number 840045 Las Vegas Nevada 89128 —
Investigational Site Number 840031 Linden New Jersey 07036 —
Investigational Site Number 840060 Hickory North Carolina 28601 —
Investigational Site Number 840064 Morganton North Carolina 28655 —
Investigational Site Number 840043 Wilmington North Carolina 28401 —
Investigational Site Number 840082 Winston-Salem North Carolina 27103 —
Investigational Site Number 840025 Oklahoma City Oklahoma 73104 —
Investigational Site Number 840022 Oklahoma City Oklahoma 73112 —
Investigational Site Number 840029 Beaver Pennsylvania 15009 —
Investigational Site Number 840056 Downingtown Pennsylvania 19335 —
Investigational Site Number 840093 Anderson South Carolina 29621 —
Investigational Site Number 840097 Greenville South Carolina 29605 —
Investigational Site Number 840070 Greer South Carolina 29651 —
Investigational Site Number 840044 North Myrtle Beach South Carolina 29582 —
Investigational Site Number 840069 Simpsonville South Carolina 29681 —
Investigational Site Number 840079 Bristol Tennessee — —
Investigational Site Number 840006 Chattanooga Tennessee 37404 —
Investigational Site Number 840088 Knoxville Tennessee 37912 —
Investigational Site Number 840077 New Tazewell Tennessee 37825 —
Investigational Site Number 840007 Dallas Texas 75230 —
Investigational Site Number 840086 Dallas Texas 75231 —
Investigational Site Number 840027 Houston Texas 77061 —
Investigational Site Number 840004 Houston Texas 77083-4436 —
Investigational Site Number 840040 Houston Texas 77090 —
Investigational Site Number 840046 Houston Texas 77095 —
Investigational Site Number 840054 Hurst Texas 76054 —
Investigational Site Number 840017 Mesquite Texas 75149 —
Investigational Site Number 840008 Missouri City Texas 77459 —
Investigational Site Number 840094 San Antonio Texas 78229-3907 —
Investigational Site Number 840009 Sugar Land Texas 77478 —
Investigational Site Number 840053 Waco Texas 76710 —
Investigational Site Number 840095 Ogden Utah 84405 —
Investigational Site Number 840032 Salt Lake City Utah 84102 —
Investigational Site Number 840024 Norfolk Virginia — —
Investigational Site Number 840020 Richmond Virginia 23219 —
Investigational Site Number 840012 Renton Washington 98055 —

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 NCT02738151, 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 Sep 14, 2018 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02738151 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →