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ABSTRACT: Introduction
Semaglutide, a new treatment option approved for the treatment of patients with type 2 diabetes mellitus, is a glucagon-like peptide-1 receptor agonist to be injected subcutaneously once weekly. This analysis used a population pharmacokinetic model of semaglutide to identify clinically relevant covariates for exposure.Methods
A total of 1612 patients with up to seven pharmacokinetic observations each were included in the analysis. All subjects had type 2 diabetes mellitus and were enrolled in one of five trials in the phase III development program for subcutaneous semaglutide once weekly (the SUSTAIN program). The treatment duration of the trials varied from 30 to 104 weeks.Results
No clinically relevant effects on the exposure were seen for sex, age, r
SUBMITTER: Carlsson Petri KC
PROVIDER: S-EPMC6064581 | biostudies-literature | 2018 Aug
REPOSITORIES: biostudies-literature