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U.S.: The Food and Drug Administration (FDA) is the primary regulatory body, ensuring the safety and efficacy of incretin mimetics like Exenatide, Liraglutide, Dulaglutide, and Semaglutide

doi: 10.1016/j.exer.2021.108664 173 West-MaysJAPinoGLovicuFJ

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A scoping approach was selected given the anticipated heterogeneity of study designs, the predominance of preclinical literature, and the limited volume of human clinical outcome data

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Dies hat jedoch in der Regel keinen Einfluss auf die Bioverfgbarkeit