Vedtofte Louise, Knop Filip K, Vilsbøll Tina
a Center for Diabetes Research , Gentofte Hospital, University of Copenhagen , Hellerup , Denmark.
b Department of Clinical Medicine, Faculty of Health and Medical Sciences , University of Copenhagen , Copenhagen , Denmark.
Expert Opin Drug Saf. 2017 Mar;16(3):387-396. doi: 10.1080/14740338.2017.1288715. Epub 2017 Feb 15.
Type 2 diabetes (T2D) is a progressive disease with increasing prevalence in most countries. The majority of patients with T2D have inadequate glycaemic control, which increases the risk of diabetic complications later in life. New therapies with improved safety profiles are required to tackle the progressive nature of T2D. Areas covered: The efficacy and safety profile of IDegLira - a once-daily, fixed-ratio combination of insulin degludec and liraglutide, a glucagon-like peptide-1 receptor agonist (GLP-1RA), for the treatment of T2D - has been extensively evaluated. IDegLira's phase 3 clinical trial programme builds upon the clinical programmes of its mono-components, and their cardiovascular outcomes trials. The results are described here, focusing on different patient populations and compared with alternative insulin regimens. Expert opinion: IDegLira provides superior glycaemic control and mitigates the primary adverse effects associated with insulin therapy (weight gain and hypoglycaemia) and GLP-1RAs (gastrointestinal side effects) with no indication of additive effects. Accordingly, co-formulations such as IDegLira are likely to be increasingly preferred over stepwise addition and titration of the individual agents in the management of T2D.
2型糖尿病(T2D)是一种在大多数国家患病率不断上升的进展性疾病。大多数T2D患者血糖控制不佳,这增加了日后发生糖尿病并发症的风险。需要有安全性更好的新疗法来应对T2D的进展特性。涵盖领域:德谷胰岛素利拉鲁肽(IDegLira)——一种每日一次的、由德谷胰岛素和胰高血糖素样肽-1受体激动剂(GLP-1RA)利拉鲁肽按固定比例组成的复方制剂——治疗T2D的疗效和安全性已得到广泛评估。IDegLira的3期临床试验项目建立在其单一组分的临床项目及其心血管结局试验的基础之上。此处描述了试验结果,重点关注不同患者群体,并与其他胰岛素治疗方案进行了比较。专家观点:IDegLira能提供更好的血糖控制,减轻与胰岛素治疗相关的主要不良反应(体重增加和低血糖)以及GLP-1RA相关的不良反应(胃肠道副作用),且无叠加效应迹象。因此,在T2D管理中,像IDegLira这样的复方制剂可能会越来越比逐步添加和滴定单一药物更受青睐。