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That's the finding of a Dutch study published Jan

Gastrointestinal adverse events were reported by 72.5% of the patients in the cagrilintidesemaglutide group and 34.4% in the placebo group, most of which were transient and mild or moderate in severity

A useful analogy often employed in educational settings compares a cells genome to a reference library

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5 Conclusions In these studies, within the limitations of small sample sizes, no clinically relevant differences were observed in cagrilintide pharmacokinetics in people with renal or hepatic impairment compared with those with normal function