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在“和谐”研究中开展了与阿必鲁肽对比的替代终点的对照临床试验。

Comparator clinical trials of surrogate endpoints with albiglutide are in HARMONY.

作者信息

Doggrell Sheila A

机构信息

a Queensland University of Technology, Brisbane, Australia.

出版信息

Expert Rev Endocrinol Metab. 2015 May;10(3):273-276. doi: 10.1586/17446651.2015.995629. Epub 2014 Dec 26.

Abstract

Evaluation of: Ahrén B, Johnson SL, Stewart M et al. HARMONY 3: 104-Week randomized, double-blind, placebo- and active-controlled trial assessing the efficacy and safety of albiglutide compared with placebo, sitagliptin, and glimepiride in patients with type 3 diabetes taking metformin. Diabetes Care 2014;37:2141-8 and Rosenstock J, Fonseca VA, Grass JL et al. Advancing basal insulin replacement in type 2 diabetes inadequately controlled with insulin glargine plus oral agents: a comparison of adding albiglutide, a weekly GLP-1 receptor agonist, versus thrice-daily prandial insulin lispro. Diabetes Care 2014;37:2317-25. Agonists of glucagon-like peptide-1 (GLP-1) receptors are used in the treatment of Type 2 diabetes. Albiglutide is a new long-acting GLP-1 receptor agonist being developed for once weekly use. This is an evaluation of two clinical trials in the HARMONY clinical trials series. HARMONY 3 compares albiglutide with sitagliptin and glimepiride in subjects with Type 2 diabetes poorly controlled with metformin, and HARMONY 6 compares albiglutide with insulin lispro in subjects poorly controlled with slow/medium release preparations of insulin. Both studies showed that albiglutide lowered HbA1c and had advantages over its comparator drugs. However, questions remain about the safety of albiglutide. Albiglutide is not being used in subjects with a history of thyroid cancer because it is not known whether this is a rare adverse effect with albiglutide. Also, the safety of albiglutide in subjects with Type 2 diabetes and high cardiovascular risk is unknown.

摘要

评估

阿赫伦B、约翰逊SL、斯图尔特M等。HARMONY 3:一项为期104周的随机、双盲、安慰剂对照和活性药物对照试验,评估与安慰剂、西他列汀和格列美脲相比,阿必鲁肽在服用二甲双胍的2型糖尿病患者中的疗效和安全性。《糖尿病护理》2014年;37:2141 - 2148以及罗森斯托克J、丰塞卡VA、格拉斯JL等。在甘精胰岛素加口服药物控制不佳的2型糖尿病中推进基础胰岛素替代治疗:添加每周一次的胰高血糖素样肽 - 1(GLP - 1)受体激动剂阿必鲁肽与每日三次的餐时胰岛素 lispro的比较。《糖尿病护理》2014年;37:2317 - 2325。胰高血糖素样肽 - 1(GLP - 1)受体激动剂用于2型糖尿病的治疗。阿必鲁肽是一种正在研发的新型长效GLP - 1受体激动剂,拟每周使用一次。这是对HARMONY临床试验系列中的两项临床试验的评估。HARMONY 3在二甲双胍控制不佳的2型糖尿病受试者中将阿必鲁肽与西他列汀和格列美脲进行比较,而HARMONY 6在胰岛素缓释/中效制剂控制不佳的受试者中将阿必鲁肽与胰岛素 lispro进行比较。两项研究均表明阿必鲁肽可降低糖化血红蛋白(HbA1c),且优于其对照药物。然而,关于阿必鲁肽的安全性仍存在疑问。有甲状腺癌病史的受试者未使用阿必鲁肽,因为尚不清楚这是否是阿必鲁肽的一种罕见不良反应。此外,阿必鲁肽在有高心血管风险的2型糖尿病受试者中的安全性未知。

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