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Clinical Trial Summary

Primary Objective: To identify a best fasting plasma glucose (FPG) target for Chinese type 2 diabetes patients using insulin glargine which can provide the highest control rate of glycated hemoglobin (HbA1c) < 7%. Secondary Objectives: The control rate of HbA1c ≤6.5% achievement. The control rate of HbA1c <7.0% in patients achieving their FPG target. The percentage of HbA1c <7% without hypoglycemia. The percentage of patients achieving the FPG target without hypoglycemia. The percentage of patients achieving the FPG target and post prandial glucose (PPG) target (2-hour post breakfast <10 mmol/L).


Clinical Trial Description

The study duration for each patient will be 27 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02545842
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date September 7, 2015
Completion date April 20, 2018

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