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首页> 外文期刊>Journal of diabetes investigation. >Efficacy, safety, and tolerability of ipragliflozin in Asian patients with type 2 diabetes mellitus and inadequate glycemic control with metformin: Results of a phase 3 randomized, placebo‐controlled, double‐blind, multicenter trial
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Efficacy, safety, and tolerability of ipragliflozin in Asian patients with type 2 diabetes mellitus and inadequate glycemic control with metformin: Results of a phase 3 randomized, placebo‐controlled, double‐blind, multicenter trial

机译:依普列净在亚洲2型糖尿病和二甲双胍血糖控制不足的患者中的疗效,安全性和耐受性:一项3期随机,安慰剂对照,双盲,多中心试验的结果

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Aims/Introduction To determine the efficacy and safety of ipragliflozin in combination with metformin in Asian patients with type 2 diabetes mellitus. Materials and Methods This phase 3, multicenter, placebo-controlled, double-blind, parallel-group study was carried out at 18 sites in Korea and 12 sites in Taiwan. After an 8-week washout period for patients using drugs other than metformin and a 2-week run-in period, patients were randomized to either 50 mg ipragliflozin or a placebo for 24 weeks while continuing metformin. Efficacy outcomes included the changes in hemoglobin A1c, fasting plasma glucose (FPG) and bodyweight from baseline to the end of treatment (with last observation carried forward). Safety outcomes included treatment-emergent adverse events. Results Between November 2011 and January 2013, 171 patients were randomized to and administered ipragliflozin ( n = 87) or a placebo ( n = 83). The mean changes (standard deviation) in hemoglobin A1c were ?0.94% (0.75%) and ?0.47% (0.81%) in the ipragliflozin and placebo groups, respectively (between-group difference ?0.46%, P Conclusions These results show that ipragliflozin is effective and well tolerated when used in combination with metformin in Asian patients with type 2 diabetes mellitus.
机译:目的/简介确定伊普列净与二甲双胍联合治疗亚洲2型糖尿病患者的疗效和安全性。材料和方法在韩国的18个站点和台湾的12个站点中进行了此第3阶段,多中心,安慰剂对照,双盲,平行组研究。对于使用除二甲双胍以外的药物的患者进行了8周的冲洗期和2周的磨合期后,在继续使用二甲双胍的情况下,将患者随机分配至50 mg依普列净或安慰剂治疗24周。疗效包括从基线到治疗结束时血红蛋白A1c,空腹血糖(FPG)和体重的变化(最后观察到的结果)。安全性结果包括治疗紧急不良事件。结果在2011年11月至2013年1月之间,有171例患者被随机分配接受伊格列净(n = 87)或安慰剂(n = 83)。依普列净和安慰剂组血红蛋白A1c的平均变化(标准差)分别为0.94%(0.75%)和0.47%(0.81%)(组间差异为0.46%,P结论)这些结果表明,依普列净与二甲双胍联合使用在亚洲2型糖尿病患者中有效且耐受性良好。

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