Takeda Development Center Americas, Inc., Deerfield, IL, USA.
Clin Pharmacol Drug Dev. 2015 May-Jun;4(3):175-83. doi: 10.1002/cpdd.170. Epub 2015 Jan 23.
This double-blind, randomized, placebo- and active-controlled, parallel group trial evaluated the potential for multiple-dose fasiglifam to prolong the QT/QTc interval in healthy adults. A total of 280 men and women aged 18-50 years were randomized to receive 14 days of fasiglifam 50 mg (n = 69), fasiglifam 400 mg (n = 70), or placebo (n = 70), or 13 days of placebo followed by single-dose moxifloxacin 400 mg (positive control; n = 71). The primary endpoint was the least square mean difference between fasiglifam and placebo in time-matched change from baseline to last dosing day in QT interval corrected using the Fridericia method (QTcF, calculated as QT/RR(0) (.333) ). For both fasiglifam doses, differences from placebo in QTcF were between -4.9 and 3.0 milliseconds at all postdose time points; maximum upper bounds of the one-sided 95% confidence interval for the difference were 5.7 milliseconds for fasiglifam 50 mg and 2.3 milliseconds for fasiglifam 400 mg, meeting predefined criteria for absence of prolongation. Alternate correction methods (Bazett and Individual) showed similar results. Fasiglifam was well tolerated; no subject withdrew due to an adverse event after receiving fasiglifam. In summary, multiple-dose fasiglifam did not affect cardiac repolarization at therapeutic and supratherapeutic doses and was well tolerated in healthy subjects.
这项双盲、随机、安慰剂和活性对照、平行组试验评估了多剂量法格列净延长健康成年人 QT/QTc 间期的潜力。总共 280 名年龄在 18-50 岁的男性和女性被随机分配接受 14 天的法格列净 50mg(n=69)、法格列净 400mg(n=70)或安慰剂(n=70),或 13 天的安慰剂,然后单剂量莫西沙星 400mg(阳性对照;n=71)。主要终点是法格列净与安慰剂在时间匹配的 QT 间期校正(使用 Fridericia 法校正的 QTcF,计算为 QT/RR(0) (.333) )从基线到最后给药日的变化的最小平方均差。对于两种法格列净剂量,在所有给药后时间点,与安慰剂相比,QTcF 的差异在-4.9 至 3.0 毫秒之间;法格列净 50mg 差异的单侧 95%置信区间上限最大为 5.7 毫秒,法格列净 400mg 的差异上限最大为 2.3 毫秒,符合无延长的预设标准。替代校正方法(Bazett 和个体)显示出相似的结果。法格列净耐受性良好;没有受试者在接受法格列净后因不良事件退出。总之,多剂量法格列净在治疗和超治疗剂量下不会影响心脏复极,在健康受试者中耐受性良好。