drugset / Trial / NCT02058160

Efficacy and Safety of the Insulin Glargine/Lixisenatide Fixed Ratio Combination Versus Insulin Glargine in Patients With Type 2 Diabetes

NCT02058160 ↗

Phase 3 Completed 736 enrolled Sanofi
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary Objective: To demonstrate the superiority of the insulin glargine/lixisenatide fixed ratio combination (FRC) to insulin glargine in glycated hemoglobin (HbA1c) change from baseline to Week 30. Secondary Objective: To compare the overall efficacy and safety of insulin glargine/lixisenatide FRC to insulin glargine (with or without metformin) over a 30 week treatment period in participants with type 2 diabetes.

Timeline

Start
2014-01
Primary completion
2015-07
Completion
2015-07

Outcome

Met primary endpoint

registry Insulin Glargine/Lixisenatide Fixed Ratio Combination vs Insulin Glargine; p <0.0001; Least square (LS) mean difference -0.52 (95% CI -0.633 to -0.397) NCT02058160 ↗

paper iGlarLixi showed greater reductions in HbA1c from baseline compared with iGlar (-1.1% vs. -0.6%, P < 0.0001) PMID 27650977 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lixisenatide Peptide 10 ug —
Subject Lixisenatide Peptide 20 ug —
Comparator insulin glargine Protein / enzyme biologic 20 iu —
Comparator insulin glargine Protein / enzyme biologic 30 iu —
Comparator insulin glargine Protein / enzyme biologic 40 iu —
Comparator insulin glargine Protein / enzyme biologic 60 iu —
Comparator insulin glargine Protein / enzyme biologic 60 iu Subcutaneous
Background Metformin Small molecule — Oral