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Description
and (3) early oxyntomodulin analogs, which were discontinued in part because regulatory endpoints for combination receptor agonism had not yet been established ( 8.1 Regulatory expectations and evidence standards Regulatory agencies increasingly emphasize mechanism-anchored development supported by robust pharmacodynamic biomarkers and clinically meaningful endpoints ( A recurring integrity issue in peptide development has been premature extrapolation from animal models to humans

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Europe Patent Number EP 2120994, 2018
