Poon Terri, Nelson Patric, Shen Larry, Mihm Michael, Taylor Kristin, Fineman Mark, Kim Dennis
Amylin Pharmaceuticals, Inc., San Diego, California 92121, USA.
Diabetes Technol Ther. 2005 Jun;7(3):467-77. doi: 10.1089/dia.2005.7.467.
Exenatide is the first of a new class of agents known as incretin mimetics that are in development for the treatment of type 2 diabetes. Exenatide has been shown to reduce fasting and postprandial glucose in patients with type 2 diabetes, as well as provide sustained reductions in hemoglobin A 1c (HbA 1c). This study was designed to assess the dose dependencies of the glucoregulatory effects and tolerability of exenatide when added to diet and exercise or metformin monotherapy in patients with type 2 diabetes.
In this randomized, triple-blinded, placebo-controlled Phase 2 clinical trial, 156 patients were randomized to placebo or exenatide at 2.5, 5.0, 7.5, or 10.0 microg administered b.i.d. for 28 days.
After 28 days of therapy, exenatide was associated with significant (P < 0.0001, linear contrast testing), dose-dependent reductions in HbA 1c (0.1 +/- 0.1%, -0.3 +/- 0.1%, -0.4 +/- 0.1%, +/-0.5 +/- 0.0%, and -0.5 +/- 0.1% for placebo and 2.5, 5.0, 7.5, and 10.0 microg b.i.d. exenatide, respectively) and significant (P = 0.0006, linear contrast testing) reductions in fasting plasma glucose (+6.8 +/- 4.1, -20.1 +/- 5.2, -21.2 +/- 3.9, -17.7 +/- 4.8, and -17.3 +/- 4.4 mg/dL for placebo and 2.5, 5.0, 7.5, and 10.0 microg b.i.d. exenatide, respectively) by Day 28. These reductions were similar for patients treated with diet/exercise and those treated with metformin. In addition, patients receiving exenatide exhibited dose-dependent reductions in body weight (0.0 +/- 0.3, -0.7 +/- 0.3, -0.7 +/- 0.2, -1.4 +/- 0.3, and -1.8 +/- 0.3 kg for placebo and 2.5, 5.0, 7.5, and 10.0 microg b.i.d. exenatide, respectively; P < 0.01 for 7.5 and 10.0 microg b.i.d. exenatide doses compared with placebo) at Day 28. The most common adverse event was mild-to-moderate nausea that was dose-dependent (seven of 123 patients randomized to exenatide withdrew from the study because of gastrointestinal effects).
Exenatide dose-dependently improved glycemic control and reduced body weight over 28 days in patients with type 2 diabetes treated with diet/exercise or metformin.
艾塞那肽是一类新型药物(称为肠促胰岛素类似物)中的首个药物,目前正处于治疗2型糖尿病的研发阶段。已证实艾塞那肽可降低2型糖尿病患者的空腹血糖和餐后血糖,并能持续降低糖化血红蛋白(HbA1c)水平。本研究旨在评估在2型糖尿病患者中,将艾塞那肽添加到饮食和运动或二甲双胍单药治疗中时,其血糖调节作用和耐受性的剂量依赖性。
在这项随机、三盲、安慰剂对照的2期临床试验中,156例患者被随机分为安慰剂组或接受每日两次、剂量分别为2.5、5.0、7.5或10.0微克的艾塞那肽治疗,为期28天。
治疗28天后,艾塞那肽与糖化血红蛋白水平显著(P<0.0001,线性对比检验)、剂量依赖性降低相关(安慰剂组及每日两次分别使用2.5、5.0、7.5和10.0微克艾塞那肽组的降低幅度分别为0.1±0.1%、-0.3±0.1%、-0.4±0.1%、-0.5±0.0%和-0.5±0.1%),且空腹血糖也显著(P = 0.0006,线性对比检验)降低(安慰剂组及每日两次分别使用2.5、5.0、7.5和10.0微克艾塞那肽组在第28天时的降低幅度分别为+6.8±4.1、-20.1±5.2、-21.2±3.9、-17.7±4.8和-17.3±4.4毫克/分升)。饮食/运动治疗的患者和接受二甲双胍治疗的患者的这些降低幅度相似。此外,接受艾塞那肽治疗的患者体重呈剂量依赖性降低(安慰剂组及每日两次分别使用2.5、5.0、7.5和10.0微克艾塞那肽组在第28天时的降低幅度分别为0.0±0.3、-0.7±0.3、-0.7±0.2、-1.4±0.3和-1.8±0.3千克;与安慰剂相比,每日两次使用7.5和10.0微克艾塞那肽剂量组P<0.01)。最常见的不良事件是轻至中度恶心,且呈剂量依赖性(123例随机接受艾塞那肽治疗的患者中有7例因胃肠道不良反应退出研究)。
在接受饮食/运动或二甲双胍治疗的2型糖尿病患者中,艾塞那肽在28天内可剂量依赖性地改善血糖控制并减轻体重。