NL-OMON45541已完成不适用
A phase I, open-label, randomized, 4-way crossover study in subjects with chronic Hepatitis B virus infection to assess pharmacokinetics (fasted/fed), safety, tolerability and pharmacodynamics of single oral doses of Farnesoid X receptor agonist EYP001a. - EYP001 study in subjects with chronic hepatitis B virus (HBV) infection
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 14
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
- •- Has documented chronic HBV infection
- •- Gender : male or female
- •- Age : 18-65 years, inclusive, at screening
- •- Body mass index (BMI) : 17.0-35.0 kg/m2 inclusive, at screening
排除标准
- •Suffering from hepatitis C, cancer or HIV/AIDS. Previous participation in the current study. In case of donating more than 100 milliliters of blood in the 60 days prior the start of this study.
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