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MK‑3577 is an orally active small molecule glucagon receptor antagonist that was developed by Merck & Co for the treatment of type 2 diabetes mellitus. The drug acts by blocking the glucagon receptor (GCGR), thereby inhibiting glucagon-mediated increases in hepatic glucose production, which is a key mechanism in the pathogenesis of type 2 diabetes. In preclinical and phase II clinical studies, MK‑3577 demonstrated efficacy in lowering blood glucose and showed an acceptable safety profile. However, development was discontinued after phase II trials[2][3][4][5].
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