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临床试验/IRCT20110523006565N2
IRCT20110523006565N2尚未招募未知

Bioequivalence Study of Ursodeoxycholic acid Tablets manufactured by Raihaneh and So-Se-Pharm Pharmaceutical companies

Kermanshah University of Medical Sciences0 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
尚未招募
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 45 years(—)
性别
All

入选标准

  • Written informed consent.
  • Normal findings in the physical examination.
  • Clinical laboratory values within 10% above or below the laboratory’s stated normal range
  • To be a non-smoker

排除标准

  • History of hypersensitivity to the study drug or related products
  • Significant history or presence of gastrointestinal, liver or kidney disease, or any other condition known to interfere with the absorption, distribution, metabolism or excretion of common medications
  • Any clinically significant illness during the 4 weeks prior to day 1 of this study
  • Maintenance therapy with any drug, or history of drug dependence, alcohol abuse, or serious neurological or psychological disease
  • Use of any systemic medication (including OTC preparations) within 14 days preceding day 1 of this study
  • HIV and Hepatitis A, B and C positive subjects

研究者

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