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If proven effective, GLP-1 RAs could become an accessible, well-tolerated option to address the inflammatory and thrombotic risks that complicate these disorders

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Research has also described a distinct potency pattern across its receptor targets: Strong GIP receptor activity (around 8.9 higher than native GIP) Moderate GLP-1 receptor activation (about 0.4 relative potency) Modest glucagon receptor activity (about 0.3 relative potency) This balanced profile provides a framework for studying coordinated metabolic responses rather than isolated single-pathway effects