JPRN-UMIN000031175已完成1 期
A randomised, first-in-human, double-blinded, placebo-controlled study to determine the safety, tolerability, pharmacokinetics, and pharmacodynamics of single and multiple ascending doses of CP1050 in healthy subjects; including the effect of food and gender on the pharmacokinetics and pharmacodynamics of a single dose of CP1050 in healthy subjects - A randomised, first-in-human, double-blinded, placebo-controlled study of CP1050 in healthy subjects
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 66
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
- 18years-old 至 55years-old(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •- Presence or history of any clinically significant disease that could interfere with the objectives of the study or the safety of the subject in the opinion of the Investigator. - Participation in more than 3 clinical studies involving administration of an IMP in the past one year, or any study within 12 weeks. - Clinically significant abnormalities in ECG or laboratory tests.
研究者
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