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Some research protocols have explored doses up to 4.5 mg weekly, which showed slightly greater efficacy in the phase 2 dose-finding trial but also increased side effect burden

[10] Because amylin signaling is a different pathway from the incretin (GLP-1) pathway, cagrilintide is attractive as a partner drug: the two mechanisms can be additive

Morning, afternoon, or evening all produce comparable pharmacokinetic profiles

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*Correspondence: Predrag Sikiric, [email protected] This article was submitted to Gastrointestinal and Hepatic Pharmacology, a section of the journal Frontiers in Pharmacology Disclaimer All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers

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