NL-OMON38936已完成不适用
Comparison of two modified release (M.R.) formulations of S16257 22.5 mg o.d, with S 16257 immediate release tablet 7.5 mg b.i.d and linearity assessment of S 16257 pharmacokinetic over 7.5, 22.5 and 30 mg o.d doses of one of the M.R. formulations An open-label, phase I, single-centre, randomised five-way crossover study in healthy participants. - S 16257 comparative PK study
Institut de Recherches Internationales Servier I.R.I.S0 个研究点目标入组 15 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 15
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •healthy male and female Caucasian subjects, non-smoking or smoking less then 10 cigarettes per day, 18 - 65 yrs, inclusive, 18.5 - 30.0 kg/m2, inclusive
排除标准
- •Suffering from hepatitis B, hepatitis C, cancer or HIV/AIDS. In case of participation in another drug study within 90 days before the start of this study or being a blood donor within 3 months from the start of the study.
研究者
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