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临床试验/JPRN-UMIN000031175
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

Curadim Pharma Co., Ltd.0 个研究点目标入组 66 人开始时间: 2018年2月14日最近更新:
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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