Katz L, Manamley N, Snyder W J, Dodds M, Agafonova N, Sierra-Johnson J, Cruz M, Kaur P, Mudaliar S, Raskin P, Kewalramani R, Pellacani A
Amgen Inc., Thousand Oaks, CA, USA.
Amgen Ltd, Cambridge, UK.
Diabetes Obes Metab. 2016 Feb;18(2):191-5. doi: 10.1111/dom.12586. Epub 2015 Dec 14.
Phase I studies have shown that AMG 151 activates glucokinase, a key enzyme in glucose homeostasis. The present randomized, placebo-controlled phase IIa study evaluated the dose-effect relationship of the glucokinase activator AMG 151 relative to placebo on fasting plasma glucose (FPG) in 236 patients (33-35 patients per arm) with type 2 diabetes treated with metformin. Patients received oral AMG 151 at 50, 100 or 200 mg twice daily, AMG 151 at 100, 200 or 400 mg once daily or matching placebo for 28 days. A significant linear dose-effect trend was observed with the twice-daily regimen (p = 0.004) for change in FPG to day 28. No trend was observed with the once-daily regimen. A higher incidence of hypoglycaemia and hypertriglyceridaemia was observed with AMG 151 administration. AMG 151 significantly reduced FPG when administered twice daily but not when administered once daily in patients with type 2 diabetes treated with metformin.
I期研究表明,AMG 151可激活葡萄糖激酶,这是葡萄糖稳态中的一种关键酶。目前这项随机、安慰剂对照的IIa期研究评估了葡萄糖激酶激活剂AMG 151相对于安慰剂对236例接受二甲双胍治疗的2型糖尿病患者空腹血糖(FPG)的剂量效应关系。患者每日两次口服50、100或200mg的AMG 151,或每日一次口服100、200或400mg的AMG 151,或服用匹配的安慰剂,持续28天。对于至第28天的FPG变化,每日两次给药方案观察到显著的线性剂量效应趋势(p = 0.004)。每日一次给药方案未观察到趋势。AMG 151给药后低血糖和高甘油三酯血症的发生率较高。在接受二甲双胍治疗的2型糖尿病患者中,AMG 151每日两次给药时可显著降低FPG,但每日一次给药时则无此效果。