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These events were generally mild to moderate in severity and included: Nausea often accompanying changes in bowel habits, particularly after dose escalation Diarrhoea loose or watery stools, sometimes with urgency Vomiting less common but reported, especially at higher doses Constipation occurring in some individuals, reflecting the variable effect on gut motility Abdominal discomfort or bloating a sensation of fullness or cramping Flatulence increased wind, which can accompany altered digestion Gastrointestinal adverse events were the most common reason for discontinuation in the Phase 2 trial, occurring in approximately 510% of participants depending on dose group

It is studied in laboratory and in vitro research for its strong affinity for copper and its role in skin- and tissue-related processes

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Opinions on GLP-1 regulation are mixed: 40% think the current rules are fair, 28% want fewer restrictions, and 22% think there should be more