MedPath

A "Real World" Trial to Determine Efficacy and Health Outcomes of Toujeo Compared to "Standard of Care" Basal Insulins in Insulin Naïve Patients Initiating Insulin

Phase 4
Completed
Conditions
Diabetes Mellitus, Type 2
Interventions
Registration Number
NCT02967224
Lead Sponsor
Sanofi
Brief Summary

Primary Objective:

To demonstrate noninferiority of Toujeo versus "standard of care" basal insulin therapy measured as glycosylated hemoglobin (HbA1c) change

Secondary Objectives:

* To demonstrate superiority of Toujeo versus "standard of care" basal insulin if noninferiority is met, measured as HbA1c change.

* To compare Toujeo to other "standard of care" basal insulin in terms of patient persistence with assigned basal insulin therapy with or without intensification.

* Risk of hypoglycemia including the incidence of documented symptomatic or severe hypoglycemic events \[as defined by the American Diabetes Association (ADA\] Workgroup on Hypoglycemia).

* Change in fasting plasma glucose (FPG).

* Change in body weight.

* Differences in patient reported outcomes measured by Diabetes Treatment Satisfaction Questionnaire Status and Change Versions (DTSQs and DTSQc).

* Change in hypoglycemic control subscale (HCS)

* Healthcare resource utilization including hospitalizations and emergency department or other health care provider visits and healthcare costs.

Detailed Description

The total study duration will be up to 55 weeks, consisting of a 1-week screening period at the site, a 26-week treatment period, and a 26-week extension period.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
705
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
"Standard of care" commercially available basal insulinNPH insulinLantus, Humulin Neutral Protamine Hagedorn (NPH), Levemir or Tresiba or other basal insulin, including biosimilar insulin will be administered once or twice daily according to label in addition to noninsulin antidiabetic agents
Toujeoinsulin glargine (U300)Toujeo will be administered once daily in addition to noninsulin antidiabetic agents
"Standard of care" commercially available basal insulininsulin glargine (U100)Lantus, Humulin Neutral Protamine Hagedorn (NPH), Levemir or Tresiba or other basal insulin, including biosimilar insulin will be administered once or twice daily according to label in addition to noninsulin antidiabetic agents
"Standard of care" commercially available basal insulininsulin degludecLantus, Humulin Neutral Protamine Hagedorn (NPH), Levemir or Tresiba or other basal insulin, including biosimilar insulin will be administered once or twice daily according to label in addition to noninsulin antidiabetic agents
"Standard of care" commercially available basal insulininsulin detemirLantus, Humulin Neutral Protamine Hagedorn (NPH), Levemir or Tresiba or other basal insulin, including biosimilar insulin will be administered once or twice daily according to label in addition to noninsulin antidiabetic agents
Primary Outcome Measures
NameTimeMethod
Change in HbA1c (percentage %)Baseline to 6 Months
Secondary Outcome Measures
NameTimeMethod
Percentage of patients whose HbA1c decreased at least 1%At Month 6 and maintained at Month 12
Proportion of patients who achieve target HbA1c (<6.5%, <7%, <7.5%,<8.0%)At Month 6 and Month 12
Time to intensificationAt Month 6 and Month 12
Proportion of patients with HbA1c target (thresholds listed above; attainment of metabolic benefit) without documented (BG <54 mg/dL [3.0 mmol/L]) symptomatic or severe hypoglycemiaAt Month 6 and Month 12
Change in HbA1c (percentage %)Baseline to Month 12
Change in fasting plasma glucoseBaseline to Month 6 and Month 12
Proportion of patients who remain on assigned basal insulin therapy before intensification (persistent with assigned therapy)At Month 6 and Month 12
Proportion of patients who remain on assigned basal insulin therapy whether intensification occurred or notAt Month 6 and Month 12
Proportion of patients with HbA1c target (thresholds listed above; attainment of metabolic benefit) without documented (blood glucose (BG) ≤70 mg/dL [3.9 mmol/L]) symptomatic or severe hypoglycemiaAt Month 6 and Month 12
Percentage of patients requiring intensificationAt Month 6 and Month 12

Trial Locations

Locations (128)

Investigational Site Number 372003

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Dublin 4, Ireland

Investigational Site Number 327002

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Dublin 7, Ireland

Investigational Site Number 250045

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Montpellier, France

Investigational Site Number 250016

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Montpellier, France

Investigational Site Number 076005

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Fortaleza, Brazil

Investigational Site Number 076010

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Taguatinga, Brazil

Investigational Site Number 076011

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São José dos Campos, Brazil

Investigational Site Number 250058

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La Rochelle Cedex 1, France

Investigational Site Number 076007

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São paulo, Brazil

Investigational Site Number 250008

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BOIS GUILLAUME Cedex, France

Investigational Site Number 250024

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Bordeaux, France

Investigational Site Number 250028

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Brest, France

Investigational Site Number 250063

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Paris, France

Investigational Site Number 250053

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Paris, France

Investigational Site Number 250014

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Caen, France

Investigational Site Number 250017

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Le Puy En Velay Cedex, France

Investigational Site Number 250009

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Venissieux, France

Investigational Site Number 076-001

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Curitiba, Brazil

Investigational Site Number 250043

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Tarbes, France

Investigational Site Number 250030

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Pierre-Bénite, France

Investigational Site Number 250025

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Corbeil Essonnes, France

Investigational Site Number 250011

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Eaubonne, France

Investigational Site Number 250034

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Lamagistere, France

Investigational Site Number 250039

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Reims Cedex, France

Investigational Site Number 250057

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Bar le Duc, France

Investigational Site Number 250050

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BETHUNE Cedex, France

Investigational Site Number 250003

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CAHORS Cedex 9, France

Investigational Site Number 250064

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CHALONS EN CHAMPAGNE Cedex, France

Investigational Site Number 250026

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Cholet, France

Investigational Site Number 076008

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Sao Paulo, Brazil

Investigational Site Number 250060

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Alencon Cedex, France

Investigational Site Number 076003

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São Paulo, Brazil

Investigational Site Number 250023

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Amiens Cedex 1, France

Investigational Site Number 250013

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La Roche Sur Yon, France

Investigational Site Number 250027

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La Seyne sur Mer, France

Investigational Site Number 724006

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Majadahonda, Spain

Investigational Site Number 724025

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Madrid, Spain

Investigational Site Number 826006

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Portsmouth, United Kingdom

Investigational Site Number 276013

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Bornheim, Germany

Investigational Site Number 250044

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Orleans, France

Investigational Site Number 076004

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Fortaleza, Brazil

Investigational Site Number 076009

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Rio de Janeiro, Brazil

Investigational Site Number 250012

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Marseille, France

Investigational Site Number 250054

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Maubeuge, France

Investigational Site Number 250020

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Montpellier, France

Investigational Site Number 250046

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Nevers, France

Investigational Site Number 250041

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Nimes, France

Investigational Site Number 250004

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NARBONNE Cedex, France

Investigational Site Number 250035

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Mulhouse, France

Investigational Site Number 250032

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Paris, France

Investigational Site Number 250005

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Paris, France

Investigational Site Number 250021

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Pierre-Bénite, France

Investigational Site Number 250052

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POITIERS Cedex, France

Investigational Site Number 250051

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PRINGY Cedex, France

Investigational Site Number 250022

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Roubaix, France

Investigational Site Number 250055

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Sete, France

Investigational Site Number 250033

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Saint-Mandé, France

Investigational Site Number 250056

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Strasbourg, France

Investigational Site Number 250031

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Strasbourg Cedex 2, France

Investigational Site Number 250001

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Strasbourg, France

Investigational Site Number 250029

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Vandoeuvre Les Nancy Cedex, France

Investigational Site Number 250002

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Toulouse Cedex 3, France

Investigational Site Number 250007

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VICHY Cedex, France

Investigational Site Number 250059

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Villeneuve sur Lot, France

Investigational Site Number 250006

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Vichy, France

Investigational Site Number 276001

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Dresden, Germany

Investigational Site Number 276016

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Hamburg, Germany

Investigational Site Number 276014

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Hohenmölsen, Germany

Investigational Site Number 276002

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Dresden, Germany

Investigational Site Number 276008

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Oldenburg, Germany

Investigational Site Number 276017

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Münster, Germany

Investigational Site Number 276006

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Pirna, Germany

Investigational Site Number 276010

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Rehlingen-Siersburg, Germany

Investigational Site Number 276005

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Riesa, Germany

Investigational Site Number 276009

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Neuwied, Germany

Investigational Site Number 276012

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Neumünster, Germany

Investigational Site Number 276011

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Schweinfurt, Germany

Investigational Site Number 276007

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Sulzbach-Rosenberg, Germany

Investigational Site Number 642001

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Bucuresti, Romania

Investigational Site Number 642002

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Bucuresti, Romania

Investigational Site Number 642005

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Galati, Romania

Investigational Site Number 642009

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Iasi, Romania

Investigational Site Number 642008

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Targoviste, Romania

Investigational Site Number 724013

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Almansa, Spain

Investigational Site Number 724016

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Barakaldo, Spain

Investigational Site Number 642006

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Oradea, Romania

Investigational Site Number 724024

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Badalona, Spain

Investigational Site Number 724019

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Barcelona, Spain

Investigational Site Number 724005

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Barcelona, Spain

Investigational Site Number 724008

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Burgos, Spain

Investigational Site Number 724017

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Barcelona, Spain

Investigational Site Number 724018

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Donostia, Spain

Investigational Site Number 724026

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Ferrol, Spain

Investigational Site Number 724014

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La Coruña, Spain

Investigational Site Number 724021

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Gerona, Spain

Investigational Site Number 724027

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Huelva, Spain

Investigational Site Number 724001

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LLeida, Spain

Investigational Site Number 724022

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Valencia, Spain

Investigational Site Number 724012

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Sabadell, Spain

Investigational Site Number 724030

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Málaga, Spain

Investigational Site Number 724028

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Madrid, Spain

Investigational Site Number 724020

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Málaga, Spain

Investigational Site Number 724011

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Sevilla, Spain

Investigational Site Number 724010

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Sevilla, Spain

Investigational Site Number 724009

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Santiago de Compostela, Spain

Investigational Site Number 724007

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Vitoria, Spain

Investigational Site Number 724002

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Valencia, Spain

Investigational Site Number 826033

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Atherstone, United Kingdom

Investigational Site Number 826008

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Bradford on Avon, United Kingdom

Investigational Site Number 826016

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Ayr, United Kingdom

Investigational Site Number 826004

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Chertsey, United Kingdom

Investigational Site Number 826011

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Chesterfield, United Kingdom

Investigational Site Number 826028

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Chippenham, United Kingdom

Investigational Site Number 826027

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Cornwall, United Kingdom

Investigational Site Number 826003

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Craigavon, United Kingdom

Investigational Site Number 826038

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Cornwall, United Kingdom

Investigational Site Number 826031

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Coventry, United Kingdom

Investigational Site Number 826035

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Dudley, United Kingdom

Investigational Site Number 826019

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Manchester, United Kingdom

Investigational Site Number 826015

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Larbert, United Kingdom

Investigational Site Number 826002

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Liverpool, United Kingdom

Investigational Site Number 826018

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Manchester, United Kingdom

Investigational Site Number 826021

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Plymouth, United Kingdom

Investigational Site Number 826009

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Nuneaton, United Kingdom

Investigational Site Number 826020

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Southampton, United Kingdom

Investigational Site Number 826013

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Taunton, United Kingdom

Investigational Site Number 642007

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Bucuresti, Romania

Investigational Site Number 642004

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Cluj-Napoca, Romania

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