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According to FDA-approved prescribing information, gastrointestinal adverse effects occur commonly with these medications, with nausea reported in 16-44% of patients, vomiting in 6-24%, and abdominal pain or distension in 5-18%, depending on the specific medication and dosage

Shift toward non-daily dosing and non-injectable routes: weekly injectables, oral tablets and pipeline transdermal/patch approaches are reducing treatment burden

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GLP-1 (Glucagon-Like Peptide-1) Delayed gastric emptying (lowers appetite and promotes extended satiation) Increased secretion of insulin Lowered glucose levels GIP (Glucose-dependent Insulinotropic Polypeptide) Increased uptake and storage of glucose Elevated fatty acid uptake Increased secretion of insulin GCG (Glucagon) Elevated lipolysis and energy expenditure Increased secretion of insulin Promotion of satiety (feeling full) Prior work on developing triple receptor agonist molecules shows a synergistic effect between GLP-1, GIP and GCG when said molecule is optimized to adequately target their respective receptors

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Semaglutide was engineered to survive far longer