IRCT20110523006565N2尚未招募未知
Bioequivalence Study of Ursodeoxycholic acid Tablets manufactured by Raihaneh and So-Se-Pharm Pharmaceutical companies
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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