Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Cell Metab. 2022 Sep 6;34(9):1234-1247.e9. doi: 10.1016/j.cmet.2022.07.013. Epub 2022 Aug 18.
With an increasing prevalence of obesity, there is a need for new therapies to improve body weight management and metabolic health. Multireceptor agonists in development may provide approaches to fulfill this unmet medical need. LY3437943 is a novel triple agonist peptide at the glucagon receptor (GCGR), glucose-dependent insulinotropic polypeptide receptor (GIPR), and glucagon-like peptide-1 receptor (GLP-1R). In vitro, LY3437943 shows balanced GCGR and GLP-1R activity but more GIPR activity. In obese mice, administration of LY3437943 decreased body weight and improved glycemic control. Body weight loss was augmented by the addition of GCGR-mediated increases in energy expenditure to GIPR- and GLP-1R-driven calorie intake reduction. In a phase 1 single ascending dose study, LY3437943 showed a safety and tolerability profile similar to other incretins. Its pharmacokinetic profile supported once-weekly dosing, and a reduction in body weight persisted up to day 43 after a single dose. These findings warrant further clinical assessment of LY3437943.
随着肥胖症的患病率不断上升,需要新的治疗方法来改善体重管理和代谢健康。正在开发的多受体激动剂可能为满足这一未满足的医疗需求提供方法。LY3437943 是一种新型三重激动肽,作用于胰高血糖素受体 (GCGR)、葡萄糖依赖性胰岛素释放肽受体 (GIPR) 和胰高血糖素样肽-1 受体 (GLP-1R)。在体外,LY3437943 表现出平衡的 GCGR 和 GLP-1R 活性,但 GIPR 活性更高。在肥胖小鼠中,LY3437943 的给药可降低体重并改善血糖控制。通过增加 GCGR 介导的能量消耗来增强体重减轻,同时减少 GIPR 和 GLP-1R 驱动的热量摄入。在一项 1 期单次递增剂量研究中,LY3437943 表现出与其他肠促胰岛素相似的安全性和耐受性特征。其药代动力学特征支持每周给药 1 次,单次给药后体重持续减轻,可持续至第 43 天。这些发现证明了进一步临床评估 LY3437943 的必要性。