Viewing Study NCT02967224



Ignite Creation Date: 2024-05-06 @ 9:22 AM
Last Modification Date: 2024-10-26 @ 12:13 PM
Study NCT ID: NCT02967224
Status: COMPLETED
Last Update Posted: 2022-04-25
First Post: 2016-11-16

Brief Title: 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
Sponsor: Sanofi
Organization: Sanofi

Study Overview

Official Title: A Twenty-six Week Randomized Open-label 2-Arm Parallel Group Real World Pragmatic Trial to Assess the Clinical and Health Outcomes Benefit of Toujeo Compared to Standard of Care Insulin for Initiating Basal Insulin in Insulin Naïve Patients With Uncontrolled Type 2 Diabetes Mellitus With 6-Month Extension
Status: COMPLETED
Status Verified Date: 2022-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: Reach-Control
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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
U1111-1170-8104 OTHER UTN None
2015-001831-18 EUDRACT_NUMBER None None