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新型磷酸二酯酶-5抑制剂 udenafil 在健康韩国年轻受试者中的安全性、耐受性和药代动力学

Safety, tolerability and pharmacokinetics of udenafil, a novel PDE-5 inhibitor, in healthy young Korean subjects.

作者信息

Kim Bo-Hyung, Lim Hyeong-Seok, Chung Jae-Yong, Kim Jung-Ryul, Lim Kyoung Soo, Sohn Dong-Ryul, Cho Joo-Youn, Yu Kyung-Sang, Shin Sang-Goo, Paick Jae-Seung, Jang In-Jin

机构信息

Departments of Pharmacology and Clinical Pharmacology, Seoul National University College of Medicine and Hospital, Seoul, Korea.

出版信息

Br J Clin Pharmacol. 2008 Jun;65(6):848-54. doi: 10.1111/j.1365-2125.2008.03107.x. Epub 2008 Mar 3.

Abstract

WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT

The phosphodiesterase (PDE) type 5 inhibitor is a widely used agent that facilitates penile erection. Udenafil is newly developed as a PDE-5 inhibitor.

WHAT THIS STUDY ADDS

This is the first study to determine the safety, tolerability and pharmacokinetics of udenafil in healthy subjects. Udenafil was safe and well tolerated in healthy Korean subjects. The AUC and C(max) of udenafil increased supraproportionally with increasing dose upon single administration, but there was no significant drug accumulation upon multiple administrations.

AIM

To evaluate the safety, tolerability and pharmacokinetics (PK) of udenafil, a novel phosphodiesterase type 5 inhibitor.

METHODS

A double-blind, randomized, placebo-controlled, dose-rising, parallel-group, single- and multiple-dose study was conducted in healthy Korean subjects. The subjects were allocated to single-dose groups of 25, 50, 100, 200 or 300 mg (eight subjects in each dose group, including two placebos), or to multiple-dose groups of 100 or 200 mg (once-daily dosing for 7 days; nine subjects in each dose group, including three placebos). Serial samples of blood and urine were collected after oral administration and the drug concentrations in plasma and urine were determined by high-performance liquid chromatography. Safety and tolerability were evaluated by monitoring clinical laboratory parameters and adverse events.

RESULTS

Udenafil reached peak plasma concentrations at 0.8-1.3 h, and then declined mono-exponentially with a terminal half-life of 7.3-12.1 h in the single-dose study. The area under the time-concentration curves (AUC) and maximum plasma concentrations (C(max)) increased supraproportionally with increasing dose in the single-dose study. During multiple dosing, a steady state was reached at 5 days and little accumulation occurred after repeated dosing for 7 days. Udenafil was generally well tolerated in these healthy subjects, and no serious adverse events occurred.

CONCLUSIONS

Udenafil was safe and well tolerated in healthy volunteers. The AUC and C(max) of udenafil increased supraproportionally with increasing dose upon single administration, but there was no significant drug accumulation upon multiple administrations.

摘要

关于该主题的已知信息

5型磷酸二酯酶(PDE)抑制剂是一种广泛使用的促进阴茎勃起的药物。乌地那非是新开发的一种PDE-5抑制剂。

本研究的新增内容

这是第一项确定乌地那非在健康受试者中的安全性、耐受性和药代动力学的研究。乌地那非在健康韩国受试者中安全且耐受性良好。单次给药时,乌地那非的AUC和C(max)随剂量增加呈超比例增加,但多次给药后无明显药物蓄积。

目的

评估新型5型磷酸二酯酶抑制剂乌地那非的安全性、耐受性和药代动力学(PK)。

方法

在健康韩国受试者中进行了一项双盲、随机、安慰剂对照、剂量递增、平行组、单剂量和多剂量研究。受试者被分配到25、50、100、200或300mg的单剂量组(每个剂量组8名受试者,包括2名安慰剂组),或100或200mg的多剂量组(每日给药1次,共7天;每个剂量组9名受试者,包括3名安慰剂组)。口服给药后采集系列血液和尿液样本,采用高效液相色谱法测定血浆和尿液中的药物浓度。通过监测临床实验室参数和不良事件评估安全性和耐受性。

结果

在单剂量研究中,乌地那非在0.8 - 1.3小时达到血浆峰浓度,然后以单指数方式下降,终末半衰期为7.3 - 12.1小时。单剂量研究中,时间 - 浓度曲线下面积(AUC)和最大血浆浓度(C(max))随剂量增加呈超比例增加。多次给药期间,第5天达到稳态,重复给药7天后几乎无蓄积。在这些健康受试者中,乌地那非总体耐受性良好,未发生严重不良事件。

结论

乌地那非在健康志愿者中安全且耐受性良好。单次给药时,乌地那非的AUC和C(max)随剂量增加呈超比例增加,但多次给药后无明显药物蓄积。

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