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临床试验/IRCT20200407046981N19
IRCT20200407046981N19招募中未知

Comparative bioequivalence study of the Omeprazole 20 mg capsules manufactured by Yas Kavir Meybod Pharmaceutical Company versus Prilosec® (AstraZeneca Company)

Yas Kavir Meybod Pharmaceutical Company0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
24

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
18 years 至 60 years(—)
性别
Male

入选标准

  • The weight limit of each volunteer should be between 60 and 100 kg.
  • All volunteers must be non-smokers.
  • They must be healthy in terms of liver, kidney, respiratory system, mental and other general health characteristics that will be assessed.
  • Candidates who have consented to the consent form.

排除标准

  • Known hypersensitivity or idiosyncratic reaction to omeprazole or any ingredients.
  • Subjects with BP = 90/60 mm/Hg or BP = 140/90 mm/Hg.
  • Regular smoker who smokes more than ten cigarettes daily.
  • Taking any medicine during two week before dosing.

研究者

发起方
Yas Kavir Meybod Pharmaceutical Company

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