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利拉鲁肽在糖尿病中的疗效与作用(LEAD™)试验

Liraglutide Effect and Action in Diabetes (LEAD™) trial.

作者信息

Madsbad Sten

机构信息

a Department of Endocrinology, Hvidovre University Hospital, Kettegaards Alle, 2650 Hvidovre Hospital, Denmark.

出版信息

Expert Rev Endocrinol Metab. 2009 Mar;4(2):119-129. doi: 10.1586/17446651.4.2.119.

Abstract

Liraglutide is the first human glucagon-like peptide-1 receptor analog, based on the structure of native glucagon-like peptide-1 with pharmacokinetic properties suitable for once-daily dosing. In the Phase II studies and the Phase III Liraglutide Effect and Action in Diabetes (LEAD™) program, liraglutide has been shown to lower glycated hemoglobin A1c to the same degree or more than other oral antidiabetic drugs. Liraglutide also induces weight loss and improves β-cell function, blood pressure and some cardiovascular risk markers. Liraglutide is well tolerated; the adverse effect most frequently reported being transient nausea. This article reviews the Phase II studies and the Phase III LEAD™ program. In May 2008, Novo Nordisk submitted a new drug application for liraglutide to the US FDA and the EMEA.

摘要

利拉鲁肽是首个基于天然胰高血糖素样肽-1结构的人胰高血糖素样肽-1受体类似物,其药代动力学特性适合每日一次给药。在II期研究和III期利拉鲁肽治疗糖尿病的疗效与作用(LEAD™)项目中,利拉鲁肽已被证明能将糖化血红蛋白A1c降低到与其他口服抗糖尿病药物相同或更高的程度。利拉鲁肽还能诱导体重减轻,并改善β细胞功能、血压和一些心血管风险指标。利拉鲁肽耐受性良好;最常报告的不良反应是短暂性恶心。本文回顾了II期研究和III期LEAD™项目。2008年5月,诺和诺德向美国食品药品监督管理局(FDA)和欧洲药品管理局(EMEA)提交了利拉鲁肽的新药申请。

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