...
首页> 外文期刊>Kidney International Reports >Safety and Tolerability Study of an Intravenously Administered Small Interfering Ribonucleic Acid (siRNA) Post On-Pump Cardiothoracic Surgery in Patients at Risk of Acute Kidney Injury
【24h】

Safety and Tolerability Study of an Intravenously Administered Small Interfering Ribonucleic Acid (siRNA) Post On-Pump Cardiothoracic Surgery in Patients at Risk of Acute Kidney Injury

机译:安全性和耐受性研究在有急性肾脏损伤风险的患者中进行心肺胸腔注射后静脉给予小干扰核糖核酸(siRNA)的安全性

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Introduction Patients undergoing on-pump cardiac surgery are at an increased risk of acute kidney injury. QPI-1002, a small interfering ribonucleic acid, is under clinical development for the prevention of acute kidney injury. The safety, tolerability, and pharmacokinetics of QPI-1002 was evaluated in this first-in-man, Phase 1 study of a small, interfering ribonucleic acid in patients at risk of acute kidney injury after on-pump cardiac surgery. Methods In this phase 1 randomized, placebo-controlled dose-escalation study, a single i.v. dose of QPI-1002 was administered in subjects undergoing on-pump cardiac surgery. Subjects received placebo ( n ?= 4), or QPI-1002 in increasing doses of 0.5 mg/kg ( n ?= 3), 1.5 mg/kg ( n ?= 3), 5 mg/kg ( n ?= 3), and 10?mg/kg ( n ?= 3). Results A total of 16 subjects were enrolled in the study. The average maximum concentration and area under the curve from the time of dosing to the last measurable concentration of QPI-1002 were generally dose proportional, indicating that exposure increased with increasing dose. The average mean residence time (mean residence time to the last measurable concentration) was 10 to 13 minutes in all 4 drug-dosing cohorts. Adverse events occurred at a similar rate in all study groups. Of the total 109 reported adverse events, the events were distributed as 26 in the placebo group and 21, 19, 24, and 19 in the QPI-1002 0.5, 1.5, 5.0, and 10.0 mg/kg groups, respectively. Eight of the 16 subjects experienced at least 1 serious adverse event: 4 (100%) in the placebo group and 4 (33.3%) in the combined QPI-1002 cohorts. Discussion QPI-1002 was rapidly eliminated from plasma. QPI-1002 was safe and well tolerated across all dose groups. Overall, no dose-limiting toxicities or safety signals were observed in the study. Further development of QPI-1002 for prophylaxis of acute kidney injury is warranted.
机译:简介接受泵内心脏手术的患者患急性肾损伤的风险增加。 QPI-1002是一种小的干扰核糖核酸,正在临床开发中,用于预防急性肾损伤。在这项首次进行的人为研究(第一阶段)研究中对QPI-1002的安全性,耐受性和药代动力学进行了评估,该研究涉及一种小型,干扰性核糖核酸,用于接受心脏泵手术后急性肾损伤风险的患者。方法在这一1期随机,安慰剂对照剂量递增研究中,单次静脉注射在接受泵上心脏手术的受试者中,给予了QPI-1002剂量。受试者以0.5 mg / kg(n = 3),1.5 mg / kg(n = 3),5 mg / kg(n = 3)的递增剂量接受安慰剂(n = 4)或QPI-1002。 ,和10?mg / kg(n?= 3)。结果共有16名受试者参加了该研究。从给药时间到最后可测量的QPI-1002浓度,曲线下的平均最大浓度和曲线下面积通常与剂量成正比,表明暴露随剂量增加而增加。在所有4个给药组中,平均平均停留时间(至最后可测量浓度的平均停留时间)为10至13分钟。在所有研究组中,不良事件的发生率均相似。在总共109个报告的不良事件中,安慰剂组的事件为26个,QPI-1002组分别为0.5、1.5、5.0和10.0 mg / kg的事件为21、19、24和19。 16名受试者中有8名经历了至少1次严重不良事件:安慰剂组4名(100%),QPI-1002合并组4名(33.3%)。讨论QPI-1002被迅速从血浆中淘汰。 QPI-1002在所有剂量组中均安全且耐受性良好。总体而言,研究中未观察到剂量限制性毒性或安全性信号。有必要进一步开发用于预防急性肾损伤的QPI-1002。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号