Type II Diabetes Mellitus Clinical Trial
Official title:
Effect of GLP-1 Receptors Agonist Lixisenatide on Postprandial Lipid Profile in Obese Type 2 Diabetic Patients
Primary Objective:
To evaluate the ability of lixisenatide to modulate postprandial hyperlipidemia in
particular, the effects on plasma changes in triglycerides.
Secondary Objectives:
The effect of lixisenatide on the following postprandial lipids: apolipoprotein (APO) B48;
free fatty acid, lipoprotein distribution, cholesterol, and low-density lipoprotein (LDL)
oxidation.
The effect of lixisenatide on chronic low-grade inflammation present in non-insulin
dependent diabetes mellitus (NIDDM) and obesity.
The effect of lixisenatide on microvascular dysfunction. To evaluate the effect of
lixisenatide on postprandial plasma glucose, insulin and C-peptide and glucagon.
Maximum study duration of approximately 2.5 months (study treatment) ± 2 days Day 0 (baseline) plus a 10-week open-label, active-controlled treatment period (Final/End-of-treatment Visit). ;
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