跳至主要内容
临床试验/JPRN-jRCT2080223770
JPRN-jRCT2080223770未知1 期

A Single-Center, Randomized, Double-Blind, Placebo-Controlled Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Multiple Dose of SCO-792 in the Healthy Adult Subjects.

SCOHIA PHARMA, Inc.0 个研究点目标入组 36 人开始时间: 2018年1月10日最近更新:

试验速览

阶段
1 期
入组人数
36

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
>= 20age old 至 <= 45age old(—)
性别
Male

入选标准

  • # The participant is aged 20 to 45 years, inclusive, at the time of informed consent.
  • # The participant weights at least 50 kg and has a body mass index between 18.5 and 25.0 kg/m2 for Japanese.

排除标准

  • # The participant has received any investigational compound within 16 weeks (112 days) prior to the dose of randomized study drug.
  • # The participant has uncontrolled, clinically significant neurologic, cardiovascular, pulmonary, hepatic, renal, metabolic, gastrointestinal, urological or endocrine disease or other abnormality, which may impact the ability of the participant to participate or potentially confound the study results.

研究者

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