Endocrinology Division, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX
Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX.
Diabetes Care. 2021 Jul;44(7):1595-1603. doi: 10.2337/dc20-2878. Epub 2021 Apr 19.
Insulin icodec is a novel once-weekly basal insulin analog. This trial investigated the efficacy and safety of icodec using different once-weekly titration algorithms.
This was a phase 2, randomized, open-label, 16-week, treat-to-target study. Insulin-naive adults ( = 205) with type 2 diabetes and HbA 7-10% while treated with oral glucose-lowering medications initiated once-weekly icodec titrations A (prebreakfast self-measured blood glucose target 80-130 mg/dL; adjustment ±21 units/week; = 51), B (80-130 mg/dL; ±28 units/week; = 51), or C (70-108 mg/dL; ±28 units/week; = 52), or once-daily insulin glargine 100 units/mL (IGlar U100) (80-130 mg/dL; ±4 units/day; = 51), all titrated weekly. Percentage of time in range (TIR) (70-180 mg/dL) during weeks 15 and 16 was measured using continuous glucose monitoring.
TIR improved from baseline (means: A, 57.0%; B, 55.2%; C, 51.0%; IGlar U100, 55.3%) to weeks 15 and 16 (estimated mean: A, 76.6%; B, 83.0%; C, 80.9%; IGlar U100, 75.9%). TIR was greater for titration B than for IGlar U100 (estimated treatment difference 7.08%-points; 95% CI 2.12 to 12.04; = 0.005). No unexpected safety signals were observed. Level 2 hypoglycemia (<54 mg/dL) was low in all groups (0.05, 0.15, 0.38, 0.00 events per patient-year of exposure for icodec titrations A, B, and C and IGlar U100, respectively), with no episodes of severe hypoglycemia.
Once-weekly icodec was efficacious and well tolerated across all three titration algorithms investigated. The results for icodec titration A (80-130 mg/dL; ±21 units/week) displayed the best balance between glycemic control and risk of hypoglycemia.
胰岛素icodec 是一种新型的每周一次基础胰岛素类似物。本试验研究了使用不同的每周一次滴定算法的 icodec 的疗效和安全性。
这是一项为期 16 周的 2 期、随机、开放标签、以目标为导向的研究。胰岛素初治的成年 2 型糖尿病患者(n=205)在接受口服降糖药物治疗时,HbA1c 为 7-10%,起始每周一次的 icodec 滴定方案 A(早餐前自我监测血糖目标 80-130mg/dL;调整±21 单位/周;n=51)、B(80-130mg/dL;±28 单位/周;n=51)或 C(70-108mg/dL;±28 单位/周;n=52),或每日一次胰岛素甘精 100 单位/毫升(IGlar U100)(80-130mg/dL;±4 单位/天;n=51),所有药物均每周滴定一次。使用连续血糖监测仪测量第 15 和第 16 周的时间百分比(TIR)(70-180mg/dL)。
TIR 从基线(平均值:A 组为 57.0%;B 组为 55.2%;C 组为 51.0%;IGlar U100 组为 55.3%)改善到第 15 和第 16 周(估计平均值:A 组为 76.6%;B 组为 83.0%;C 组为 80.9%;IGlar U100 组为 75.9%)。B 组的 TIR 高于 IGlar U100 组(估计治疗差异 7.08%;95%CI 2.12-12.04;=0.005)。未观察到意外的安全性信号。所有组的低血糖(<54mg/dL)发生率均较低(icodec 滴定 A、B 和 C 组和 IGlar U100 组的患者年暴露事件分别为 0.05、0.15、0.38 和 0.00 次),且无严重低血糖事件发生。
在所有三种研究的滴定方案中,每周一次的 icodec 均有效且耐受性良好。A 组(80-130mg/dL;±21 单位/周)的结果在血糖控制和低血糖风险之间显示出最佳平衡。