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Among those who recovered and later increased their dose back to 7.2 mg, nearly half (45%) experienced dysesthesia again

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The development of novel dual- or triple-receptor agonists that bind to the receptors not only for GLP-1 but also to the receptors for glucose-dependent insulinotropic polypeptide (GIP) and/or glucagon is intended to address different metabolic pathways for carbohydrate, lipid, and protein metabolism simultaneously

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