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Each subject received in a random order a single subcutaneous dose of 1.2 mg liraglutide and placebo at an interval of 48 h, with subsequent clinical follow-up in the metabolic ward, during which blood pressure was monitored for the following 24-h and 24 h urinary samples were collected to assess sodium excretion

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Risk of kidney failure in patients with cancer: a south Korean population-based cohort study

Tirzepatide, as a fully approved dual GLP-1/GIP agonist, has already transformed clinical practice and set a new benchmark for pharmacological weight management