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Subtle ****-specific differences have been observed in metabolic phenotyping and PPP. We herein show that a recently developed unimolecular GLP-1/GIP co-agonist is more efficient in improving metabolic disease than either mono-agonist in both ****es. PPP led to the identification of a ****-independent protein panel with the potential to monitor non-invasively the treatment efficacies on metabolic function of this clinically advancing GLP-1/GIP co-agonist. We herein show that a recently developed unimolecular GLP-1/GIP co-agonist is more eff
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