Pharmacokinetics of sugammadex in subjects with moderate and severe renal impairment

被引:22
|
作者
Min, K. Chris [1 ]
Lasseter, Kenneth C. [2 ]
Marbury, Thomas C. [3 ]
Wrishko, Rebecca E. [1 ]
Hanley, William D. [1 ,4 ]
Wolford, Dennis G. [1 ]
de Haes, Joanna Udo [5 ]
Reitmann, Christina [1 ]
Gutstein, David E. [1 ]
机构
[1] Merck & Co Inc, Kenilworth, NJ USA
[2] Clin Pharmacol Miami Inc, Miami, FL USA
[3] Orlando Clin Res Ctr, Orlando, FL USA
[4] Genentech Inc, San Francisco, CA USA
[5] MSD, Oss, Netherlands
关键词
neuromuscular block; neuromuscular block antagonism; renal insufficiency; rocuronium; vecuronium; INDUCED NEUROMUSCULAR BLOCK; RELAXANT BINDING-AGENT; ROCURONIUM; REVERSAL; SAFETY; MULTICENTER; EFFICACY; CLEARANCE; ORG-25969; FAILURE;
D O I
10.5414/CP203025
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims: Sugammadex rapidly reverses moderate and deep rocuronium-or vecuronium-induced neuromuscular blockade at doses of 4 mg/kg and 2 mg/kg, respectively. Sugammadex is renally eliminated. This study evaluated the pharmacokinetics of sugammadex in subjects with renal impairment versus those with normal renal function. Methods: This open-label, two-part, phase 1 study included adults with moderate (creatinine clearance (CLcr) 30 < 50 mL/min) and severe (CLcr < 30 mL/min) renal impairment and healthy controls (CLcr >= 80 mL/min). A single intravenous (IV) bolus injection of sugammadex 4 mg/kg was administered into a peripheral vein over 10 seconds directly by straight needle in part 1 (n = 24; 8/group), and via an IV catheter followed by a saline flush in part 2 (n = 18; 6/group). Plasma concentrations of sugammadex were collected after drug administration. Due to dosing issues in part 1, pharmacokinetic parameters were determined for part 2 only. Safety was assessed throughout the study. Results: Pharmacokinetic data were obtained from 18 subjects. Mean sugammadex exposure (AUC(0-infinity)) in subjects with moderate and severe renal impairment was 2.42- and 5.42-times, respectively, that of healthy controls. Clearance decreased and apparent terminal half-life was prolonged with increasing renal dysfunction. Similar Cmax values were observed in subjects with renal impairment and healthy controls. There were no serious adverse events. Conclusions: Sugammadex exposure is increased in subjects with moderate and severe renal insufficiency due to progressively decreased clearance as a function of worsening renal function. Sugammadex 4 mg/kg was well tolerated in subjects with renal impairment, with a safety profile similar to that of healthy subjects. These results indicate that dose adjustment of sugammadex is not required in patients with moderate renal impairment; however, current safety experience is insufficient to support the use of sugammadex in patients with CLcr < 30 mL/min.
引用
收藏
页码:746 / 752
页数:7
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