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In laboratory and translational models, cagrilintide is therefore used to explore how peptide-mediated signaling affects glucose metabolism, energy regulation, and cross-talk between appetite pathways and peripheral metabolic tissues [4][6]

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Preclinical studies with SAR425899 clearly demonstrated dual receptor agonism in vitro and in preclinical in vivo studies, with a higher potency for the GLP1R than for the glucagon receptor in order to counterbalance the GCGR mediated increase of blood glucose levels through GLP-1 agonism 11,12,13