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