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Its binding profile is deliberately imbalanced, showing strong affinity for the GIP receptor with an EC50 of 22.4 pM while demonstrating roughly five times weaker GLP-1 receptor activation compared to native GLP-1, with an EC50 of 934 pM versus 70.5 pM for the endogenous hormone

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Some dosing and safety instructions to consider: Rotate the injection site regularly to avoid bruising, tissue damage or irritation