[authors missed]. Research Progress in the Application of Mazdutide in the Obese Population. 2026. biomedRxiv.202604.00089
Research Progress in the Application of Mazdutide in the Obese Population
DOI: 10.12201/bmr.202604.00089
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Abstract: As the first dual agonist targeting both glucagon-like peptide-1 (GLP-1) and glucagon (GCG) receptors, Mazdutide exerts significant weight loss effects through multiple mechanisms including delayed gastric emptying, enhanced satiety, suppressed appetite, and regulation of energy metabolism. In individuals with simple overweight or obesity, multiple clinical trials have demonstrated that Mazdutide can significantly reduce body weight, waist circumference, and body mass index (BMI), while improving metabolic indicators such as blood glucose, blood lipids, and blood pressure. The weight loss effect is dose-dependent. In populations with obesity and type 2 diabetes, Mazdutide also shows significant dual benefits in weight reduction and glucose lowering, with efficacy superior to some drugs of the same class and a safety profile similar to traditional GLP-1 receptor agonists. Common adverse reactions are mainly gastrointestinal, mostly mild to moderate, and more frequent during the dose escalation phase. Furthermore, clinical studies on Mazdutide in areas such as polycystic ovary syndrome and postoperative adjuvant therapy are underway, demonstrating its broad application potential. Overall, Mazdutide provides an effective and convenient pharmacological option for patients with obesity or overweight, particularly suitable for adults with poor response to lifestyle interventions and accompanying metabolic abnormalities. This article reviews the mechanism of action, pharmacokinetic characteristics, clinical efficacy, and safety profile of Mazdutide.
Key words: Mazdutide; dual receptor agonist; obesity or overweight; loss weightSubmit time: 10 April 2026
Copyright: The copyright holder for this preprint is the author/funder, who has granted biomedRxiv a license to display the preprint in perpetuity. -
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ID Submit time Number Download 1 2026-03-30 10.12201/bmr.202604.00089V1
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