Kersemaekers Wendy M, van Iersel Thijs, Nassander Ulla, O'Mara Edward, Waskin Hetty, Caceres Maria, van Iersel Marlou L P S
Merck Sharp & Dohme, Oss, Netherlands.
Celgene, Summit, New Jersey, USA.
Antimicrob Agents Chemother. 2015 Feb;59(2):1246-51. doi: 10.1128/AAC.04223-14. Epub 2014 Dec 15.
This study evaluated the safety, tolerability, and pharmacokinetics of a posaconazole i.v. (intravenous) solution. This was a single-center, 2-part, randomized, rising single- and multiple-dose study in healthy adults. In part 1, subjects received 0 (vehicle), 50, 100, 200, 250, or 300 mg posaconazole in a single dose i.v. by 30-min peripheral infusion (6 cohorts of 12 subjects each [9 active and 3 placebo], making a total of 72 subjects). Blood samples were collected until 168 h postdose. In part 2, subjects were to receive 2 peripheral infusions at a 12-h interval on day 1 followed by once-daily infusion for 9 days. However, part 2 was terminated early because of high rates of infusion site reactions with multiple dosing at the same infusion site. The pharmacokinetics results for part 1 (n=45 subjects) showed that the mean posaconazole exposure (area under the concentration-time curve from time zero to infinity [AUC0-∞]) ranged from 4,890 to 46,400 ng · h/ml (range of coefficient of variation values, 26 to 50). The dose-proportionality slope estimate (90% confidence interval) for AUC0-∞ was 1.30 (1.19 to 1.41), indicating a greater-than-dose-proportional increase. The data for safety in part 1 show that 29/72 subjects had ≥1 adverse event. Infusion site reactions were reported in 2/9 vehicle subjects, 0/18 placebo subjects, and 7/45 i.v. posaconazole subjects. The data for safety in part 2 show that infusion site reactions were reported in 1/4 (25%) placebo subjects, 3/9 (33%) vehicle control subjects, and 4/5 (80%) i.v. posaconazole (100 mg) subjects (3 posaconazole recipients subsequently developed thrombophlebitis and were discontinued from treatment). In conclusion, the posaconazole i.v. solution showed a greater-than-dose-proportional increase in exposure, primarily at doses below 200 mg. When administered peripherally at the same infusion site, multiple dosing of i.v. posaconazole led to unacceptably high rates of infusion site reactions. Intravenous posaconazole was otherwise well tolerated. Single doses of i.v. posaconazole were tolerated when given through a peripheral vein over 30 min.
本研究评估了泊沙康唑静脉溶液的安全性、耐受性和药代动力学。这是一项在健康成年人中进行的单中心、两部分、随机、单剂量递增和多剂量递增研究。在第1部分中,受试者通过30分钟外周静脉输注接受单次静脉注射0(赋形剂)、50、100、200、250或300 mg泊沙康唑(每组12名受试者,共6组[9名活性药物组和3名安慰剂组],总计72名受试者)。给药后采集血样直至168小时。在第2部分中,受试者在第1天每隔12小时接受2次外周静脉输注,随后每天输注1次,共9天。然而,由于在同一输注部位多次给药导致输注部位反应发生率较高,第2部分提前终止。第1部分(n = 45名受试者)的药代动力学结果显示,泊沙康唑的平均暴露量(从零时间到无穷大的浓度-时间曲线下面积[AUC0-∞])范围为4890至46400 ng·h/ml(变异系数值范围为26%至50%)。AUC0-∞的剂量比例斜率估计值(90%置信区间)为1.30(1.19至1.41),表明增加幅度大于剂量比例。第1部分的安全性数据显示,72名受试者中有29名发生≥1次不良事件。在2/9名接受赋形剂的受试者、0/18名接受安慰剂的受试者和7/45名接受静脉注射泊沙康唑的受试者中报告了输注部位反应。第2部分的安全性数据显示,在1/4(25%)接受安慰剂的受试者、3/9(33%)接受赋形剂对照的受试者和4/5(80%)接受静脉注射泊沙康唑(100 mg)的受试者中报告了输注部位反应(3名接受泊沙康唑的受试者随后发生血栓性静脉炎并停止治疗)。总之,泊沙康唑静脉溶液的暴露量增加幅度大于剂量比例,主要发生在低于200 mg的剂量时。当在同一输注部位进行外周给药时,静脉注射泊沙康唑多次给药导致输注部位反应发生率高得令人无法接受。否则,静脉注射泊沙康唑耐受性良好。通过外周静脉在30分钟内给予单次静脉注射泊沙康唑时耐受性良好。