Velocity Clinical Research at Medical City, Dallas, TX 75230, USA.
Lilly Diabetes and Obesity, Eli Lilly and Company, Indianapolis, IN 46225, USA.
Endocr Rev. 2024 May 7;45(3):379-413. doi: 10.1210/endrev/bnad037.
Basal insulin continues to be a vital part of therapy for many people with diabetes. First attempts to prolong the duration of insulin formulations were through the development of suspensions that required homogenization prior to injection. These insulins, which required once- or twice-daily injections, introduced wide variations in insulin exposure contributing to unpredictable effects on glycemia. Advances over the last 2 decades have resulted in long-acting, soluble basal insulin analogues with prolonged and less variable pharmacokinetic exposure, improving their efficacy and safety, notably by reducing nocturnal hypoglycemia. However, adherence and persistence with once-daily basal insulin treatment remains low for many reasons including hypoglycemia concerns and treatment burden. A soluble basal insulin with a longer and flatter exposure profile could reduce pharmacodynamic variability, potentially reducing hypoglycemia, have similar efficacy to once-daily basal insulins, simplify dosing regimens, and improve treatment adherence. Insulin icodec (Novo Nordisk) and insulin efsitora alfa (basal insulin Fc [BIF], Eli Lilly and Company) are 2 such insulins designed for once-weekly administration, which have the potential to provide a further advance in basal insulin replacement. Icodec and efsitora phase 2 clinical trials, as well as data from the phase 3 icodec program indicate that once-weekly insulins provide comparable glycemic control to once-daily analogues, with a similar risk of hypoglycemia. This manuscript details the technology used in the development of once-weekly basal insulins. It highlights the clinical rationale and potential benefits of these weekly insulins while also discussing the limitations and challenges these molecules could pose in clinical practice.
基础胰岛素仍然是许多糖尿病患者治疗的重要组成部分。最初,人们试图通过开发混悬液来延长胰岛素制剂的作用时间,这些混悬液在注射前需要进行匀化。这些胰岛素需要每天注射一次或两次,导致胰岛素暴露的变化很大,从而导致血糖控制效果不可预测。过去 20 年来的进展带来了长效、可溶性基础胰岛素类似物,其药代动力学暴露时间延长且变异性较小,提高了它们的疗效和安全性,尤其是通过减少夜间低血糖。然而,由于担心低血糖和治疗负担等多种原因,许多患者对每日一次的基础胰岛素治疗的依从性和持久性仍然较低。具有更长和平坦暴露特征的可溶性基础胰岛素可能会降低药效学变异性,潜在地降低低血糖风险,具有与每日一次基础胰岛素类似的疗效,简化给药方案,并提高治疗依从性。icodec(诺和诺德)和 insulin efsitora alfa(基础胰岛素 Fc [BIF],礼来公司)是两种设计用于每周一次给药的胰岛素,它们有可能在基础胰岛素替代方面取得进一步进展。icodec 和 efsitora 2 期临床试验以及 3 期 icodec 计划的数据表明,每周一次的胰岛素可提供与每日一次类似物相当的血糖控制,低血糖风险相似。本文详细介绍了开发每周一次基础胰岛素所使用的技术。它强调了这些每周一次胰岛素的临床原理和潜在益处,同时还讨论了这些分子在临床实践中可能带来的局限性和挑战。