NL-OMON36756已完成不适用
A Single dose, two-way crossover study of the bioequivalence of two formulations of Ribavirin - BE of Ribavirin
Schering-Plough0 个研究点目标入组 54 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
- 54
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
- •18-55 years,
- •BMI 18-30 kg/m2 (inclusive)
- •man or postmenopausal women
排除标准
- •Suffering from: hepatitis B, cancer or HIV/Aids. In case of participation in another drug study within 60 days before the start of this study or being a blood donor within 60 days from the start of the study. In case of donating more than 1.5 liters of blood (for men) / more than 1.0 liters of blood (for women) in the 10 months preceding the start of this study.
研究者
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