跳至主要内容
临床试验/NCT00489450
NCT00489450已完成1 期

Clinical Trial to Investigate the Influence of Alcohol on the Pharmacokinetics and Safety of SK3530 in Healthy Male Volunteers

SK Chemicals Co., Ltd.2 个研究点 分布在 2 个国家目标入组 18 人开始时间: 2007年3月最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
18
试验地点
2
主要终点
PK parameters - AUC, Cmax

研究概览

简要总结

This study was designed to investigate the alcohol effect of SK3530 on the pharmacokinetics (PKs) and safety.

详细描述

This study was a randomized, open, single-dose, three-treatment, three-period, three-sequence, crossover study in which subjects were received, in random order, SK3530 100mg alone, 0.5g/Kg of alcohol alone, and SK3530 plus alcohol together. There was a minimum of a 7 day washout period between treatments. The alcohol was diluted to 240 mL with water. The contents were drunk in 1 minutes or less. For SK3530 and metabolite measurement, plasma samples were collected at pre-scheduled time and the safety was monitored all through the study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • ages 20 to 50
  • body weight of IBM ± 20%

排除标准

  • cardiovascular disease
  • color-blindness or weakness
  • no availability to intake 0.5 g/Kg alcohol
  • abnormal supine blood preesure

结局指标

主要结局

PK parameters - AUC, Cmax

时间窗: 24hr after administration

次要结局

  • Safety (Vital signs, Adverse events)(until post-study visit)

研究者

申办方类型
Industry

研究点 (2)

Loading locations...

相似试验

Phase I Study to Investigate the Alcohol Interaction... | 临床试验