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ABSTRACT: Introduction
Real-world evidence on lixisenatide in Japanese people with type 2 diabetes (T2D) is lacking. Therefore, the 3-year post-marketing PRANDIAL study was conducted to evaluate the safety (primary objective) and effectiveness (secondary objective) of lixisenatide in Japanese people with T2D during routine clinical practice.Methods
This prospective, observational, multicenter, open-label study was conducted in Japanese individuals with T2D who initiated lixisenatide treatment between March 2014 and June 2017. Using electronic case report forms, investigators collected baseline demographic and clinical information and data on medications, safety and effectiveness up to 3 years after initiation of lixisenatide.Results
Overall, 3046 participants were analyzed; t
SUBMITTER: Terauchi Y
PROVIDER: S-EPMC9122860 | biostudies-literature | 2022 Jun
REPOSITORIES: biostudies-literature