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临床试验/IRCT20200407046981N4
IRCT20200407046981N4招募中未知

Randomized, single-dose, crossover comparative bioequivalence study of the Imatinib 100 mg capsules produced by Kimia pharmaceutical Co versus Gleveec® (NOVARTIS company) in 18 healthy males under fasting conditions

Kimia pharmaceutical Co0 个研究点目标入组 18 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
18

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 for each volunteer is between 60 and 100 kg.
  • Only non-smokers are allowed to participate.
  • They must be healthy in terms of liver and kidney status, respiratory system, and other general health characteristics that will be assessed.

排除标准

  • Known hypersensitivity or idiosyncratic reaction to Imatinib or any ingredients.
  • Subjects with BP = 90/60 mm/Hg or BP = 140/90 mm/Hg Any evidence of impairment of renal, hepatic, cardiac, lung or gastrointestinal function or a history of TB, epilepsy, asthma (during past 5 years), DM, psychosis or glaucoma.
  • Regular smoker who smokes more than ten cigarettes daily.
  • Taking any medicine during two week before dosing.

研究者

发起方
Kimia pharmaceutical Co

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