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临床试验/ACTRN12616000117415
ACTRN12616000117415已完成1 期

A single dose, randomized, blinded, bioequivalence study of a test formulation of clobazam tablet in a 2 way crossover comparison against the innovator clobazam tablet conducted under fasting conditions in healthy male and female volunteers

Zenith Technology Corp Ltd0 个研究点目标入组 33 人开始时间: 2016年2月3日最近更新:

试验速览

阶段
1 期
状态
已完成
入组人数
33

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 55 Years(—)
性别
All

入选标准

  • Healthy male and non-pregnant females
  • Aged between 18 and 55
  • Non-smoker
  • BMI between 18 and 30 inclusive
  • Normal, healthy individuals as determined by medical history, physical examination, ECG, blood pressure and laboratory tests
  • Able to provide written informed consent

排除标准

  • Any history of recent recurrent attacks of bronchitis, asthma, migraine headaches
  • Concomitant drug therapy of any kind
  • Sensitivity to clobazam or any other similar class of medicines, or the excipients of clobazam
  • History of any conditions that might interfere with the absorption, distribution, metabolism or excretion of the drug
  • Females who are pregnant and/or are breastfeeding
  • Smoker (anyone who has smoked in the last 6 months)
  • History of alcohol or drug abuse or dependency
  • Participation in a drug study within 60 days of the start of the study or donated blood in the 60 days preceding the study.
  • Volunteers for whom the Clinical Investigator believes, for any reason, that participation would not be an acceptable risk

研究者

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