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Its simultaneous activation of three receptor pathways GLP-1R for appetite suppression and insulin secretion, GIPR for augmented insulin response and central appetite modulation, and GCGR for energy expenditure and hepatic fat mobilisation produces metabolic effects that exceed what single or dual agonism can achieve [4][8][9]
You cannot achieve Safety Mode in the nervous system while your body is in a state of energy deficit
If evoke/evoke+ were to confirm such an effect size, it would position semaglutide as a novel modality offering several potential advantages over anti-amyloid therapies such as Lillys donanemab, e.g., oral formulation, simpler diagnostics, likely no need for PET scan monitoring
It could even mean buying out the patent for semaglutide from Novo Nordisk, or buying out the drug company altogether
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