Ontology highlight
ABSTRACT: Objective
To compare the efficacy and safety of the once-daily prandial glucagon-like peptide-1 receptor agonist lixisenatide with the dipeptidyl peptidase-4 inhibitor sitagliptin in patients aged <50 years affected by obesity and type 2 diabetes mellitus (T2DM).Materials and methods
This was a 24-week, double-blind, randomized, parallel-group study. Obese patients with T2DM inadequately controlled on metformin were randomized to lixisenatide 20 μg once-daily injection (n = 158) or once-daily oral sitagliptin 100 mg (n = 161). The primary endpoint was the proportion of patients with a glycated hemoglobin (HbA1c) <7% and ≥5% weight loss at 24 weeks.Results
The proportion of patients that achieved the primary endpoint was 12.0% for lixisenatid
SUBMITTER: Van Gaal L
PROVIDER: S-EPMC5685032 | biostudies-literature | 2014 Jun
REPOSITORIES: biostudies-literature