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Advances in peptide engineering over the last decade have led to the design of multi-agonist molecules targeting combinations of GLP-1, glucose-dependent insulinotropic polypeptide (GIP), glucagon, amylin, and peptide YY (PYY) receptors
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“While we are disappointed to discontinue the development of danuglipron, we remain committed to evaluating and advancing promising programs to bring innovative new medicines to patients,” said Dr
