TCTR20151106002已完成未知
In Vivo Bioequivalence Study of 24 mg Betahistine dihydrochloride Tablets in Healthy Thai Volunteers
Somruedee Chatsiricharoenkul0 个研究点目标入组 24 人开始时间: 2015年11月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 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 45 Years（—）
- 性别
- All
入选标准
- •Healthy Thai volunteers with a body mass index between 18-25 kg/m2
- •In good physical condition by clinical screening included history taking, physical examination and the following laboratory tests: complete blood count, blood urea nitrogen, serum creatinine, aspartate aminotransferase, alanine aminotransferase, total bilirubin, alkaline phosphatase, fasting blood sugar, urinalysis and hepatitis B surface antigen.
排除标准
- •- Pregnant or lactating women or positive pregnancy test women
- •- Allergy to the study drug
- •- Volunteers who used any drugs, food supplements, vitamins, mineral, herbal remedies, contraceptives hormonal within 14 days before study participation
研究者
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