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临床试验/NCT02515864
NCT02515864已完成2 期

A Crossover Study to Assess the Effects of FYU-981 on the QT/QTc Interval in Healthy Male and Female Volunteers

Fuji Yakuhin Co., Ltd.0 个研究点目标入组 48 人开始时间: 2015年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
48
主要终点
QT/QTc Interval

研究概览

简要总结

A Placebo-controlled, Four Way Crossover Study to Investigate the Effect on QT/QTc Interval of a Single Dose of FYU-981, Compared with Placebo, Using Moxifloxacin as a Positive Control, in Healthy Male and Female Volunteers.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Japanese adult subjects
  • Body mass index: >=18.5 and <27.5

排除标准

  • Subjects with any disease or any history of diseases that might be unsuitable for participation in the clinical study

研究组 & 干预措施

FYU-981 anticipated therapeutic dose

Experimental

Drug: FYU-981, FYU-981 Placebo, Moxifloxacin Placebo (Oral)

干预措施: Moxifloxacin Placebo (Drug)

FYU-981 supratherapeutic dose

Experimental

Drug: FYU-981, Moxifloxacin Placebo (Oral)

干预措施: FYU-981 (Drug)

FYU-981 supratherapeutic dose

Experimental

Drug: FYU-981, Moxifloxacin Placebo (Oral)

干预措施: Moxifloxacin Placebo (Drug)

FYU-981 anticipated therapeutic dose

Experimental

Drug: FYU-981, FYU-981 Placebo, Moxifloxacin Placebo (Oral)

干预措施: FYU-981 (Drug)

FYU-981 anticipated therapeutic dose

Experimental

Drug: FYU-981, FYU-981 Placebo, Moxifloxacin Placebo (Oral)

干预措施: Placebo (Drug)

Placebo

Placebo Comparator

Drug: FYU-981 Placebo, Moxifloxacin Placebo (Oral)

干预措施: Placebo (Drug)

Placebo

Placebo Comparator

Drug: FYU-981 Placebo, Moxifloxacin Placebo (Oral)

干预措施: Moxifloxacin Placebo (Drug)

Moxifloxacin

Active Comparator

Drug: Moxifloxacin, FYU-981 Placebo (Oral)

干预措施: Placebo (Drug)

Moxifloxacin

Active Comparator

Drug: Moxifloxacin, FYU-981 Placebo (Oral)

干预措施: Moxifloxacin (Drug)

结局指标

主要结局

QT/QTc Interval

时间窗: 24 hours

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

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