NL-OMON36943已完成不适用
A Single-Center, Randomized, Investigator/Subject-Blind, Adaptive Single Ascending-Dose, Placebo-Controlled, Parallel Study to Investigate the Safety, Tolerability, Pharmacokinetics (Including the Effect of Food), and Pharmacodynamics of RO5545965 Following Oral Administration in Healthy Subjects. - RO5545965 SAD and FE study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 92
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 subjects
- •18-45 yrs, inclusive
- •BMI 18 to 30 kg/m2, inclusive
- •Light smokers or non-smokers
排除标准
- •Suffering from hepatitis B, hepatitis C, cancer or HIV/AIDS.
- •Participation in another drug study within 90 days before screening, as calculated from the day of follow-up from the previous study.
- •Any donation of blood or significant blood loss within 3 months prior to first administration of the study drug.
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