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泊沙康唑的耐受性和安全性概况:对18项健康志愿者对照研究的评估。

Tolerability and safety profile of posaconazole: evaluation of 18 controlled studies in healthy volunteers.

作者信息

Moton A, Krishna G, Wang Z

机构信息

Schering-Plough Research Institute, Kenilworth, NJ 07033, USA.

出版信息

J Clin Pharm Ther. 2009 Jun;34(3):301-11. doi: 10.1111/j.1365-2710.2009.01055.x.

Abstract

BACKGROUND AND OBJECTIVES

Antifungal agent utility can be limited by safety and tolerability concerns. Posaconazole is an extended-spectrum triazole antifungal agent for the treatment and prophylaxis of invasive fungal infection. The aim was to analyse the overall safety profile of posaconazole in healthy volunteers.

METHODS

Safety data from all 18 clinical pharmacology single- and multiple-dose trials of posaconazole conducted in healthy volunteers plus 2 additional healthy subsets from other pharmacology trials were pooled and analysed. Four hundred and forty-nine healthy volunteers (354 men; 95 women) were enrolled. Three hundred and twenty-seven were white, and the mean age and weight of subjects were similar across all dosing groups. The population evaluated had no confounding factors of underlying disease or concomitant medications. Safety evaluations included spontaneously reported adverse events, clinical laboratory test results, electrocardiograms and vital sign measurements.

RESULTS

A total of 448 subjects received posaconazole, 50-1200 mg/day administered as single or multiple doses for up to 14 days. Two hundred and seventeen subjects received >or=800 mg/day posaconazole, and 188 subjects received multiple doses of posaconazole at 800 mg/day. Two hundred and thirty-one subjects received <800 mg/day. Forty-eight subjects from three studies received placebo. The incidence of treatment-emergent adverse events reported with posaconazole was similar to that seen with placebo (57% vs. 63% respectively) and unrelated to dose. The most common treatment-related adverse events (posaconazole vs. placebo) were headache (17% vs. 13%), dry mouth (9% vs. 0%) and dizziness (6% vs. 2%). No clinically significant changes in vital signs or laboratory test parameters were observed, except for transient, mild to moderate elevations in liver function test results. Posaconazole also demonstrated minimal potential to prolong corrected QT interval.

CONCLUSIONS

The safety profile analysis found posaconazole to be well tolerated, and results were similar across sex, age and race.

摘要

背景与目的

抗真菌药物的应用可能会受到安全性和耐受性问题的限制。泊沙康唑是一种用于治疗和预防侵袭性真菌感染的广谱三唑类抗真菌药物。本研究旨在分析泊沙康唑在健康志愿者中的总体安全性。

方法

汇总并分析了在健康志愿者中进行的所有18项泊沙康唑临床药理学单剂量和多剂量试验以及来自其他药理学试验的另外2个健康亚组的安全性数据。共纳入449名健康志愿者(354名男性;95名女性)。其中327名是白人,所有给药组受试者的平均年龄和体重相似。所评估的人群没有潜在疾病或合并用药等混杂因素。安全性评估包括自发报告的不良事件、临床实验室检查结果、心电图和生命体征测量。

结果

共有448名受试者接受了泊沙康唑治疗,剂量为50 - 1200 mg/天,单剂量或多剂量给药,最长达14天。217名受试者接受的泊沙康唑剂量≥800 mg/天,188名受试者接受800 mg/天的泊沙康唑多剂量给药。231名受试者接受的剂量<800 mg/天。来自三项研究的48名受试者接受了安慰剂治疗。泊沙康唑报告的治疗中出现的不良事件发生率与安慰剂相似(分别为57%和63%),且与剂量无关。最常见的与治疗相关的不良事件(泊沙康唑组与安慰剂组相比)为头痛(17%对13%)、口干(9%对0%)和头晕(6%对2%)。除肝功能检查结果有短暂的轻度至中度升高外,未观察到生命体征或实验室检查参数有临床意义的变化。泊沙康唑延长校正QT间期的可能性也极小。

结论

安全性分析发现泊沙康唑耐受性良好,且在性别、年龄和种族方面结果相似。

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