IRCT20180620040164N35已完成未知
Comparative bioequivalence study of Betahistine 16 mg tablet of ACTOVERCO and Abbott in 24 healthy male under fasting
Actover Pharmaceutical Co.0 个研究点目标入组 24 人开始时间: 待定最近更新:
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
- 20 years 至 45 years(—)
- 性别
- Male
入选标准
- •Healthy subjects (male) between 20 – 45 years of age and Body Mass Index (BMI) within 15% of normal range according to the accepted normal values between 18.5 and 30 (inclusive), calculated as kg/m2.
- •Subjects with no significant diseases or clinically significant abnormal findings during screening, medical history, clinical examination and laboratory evaluations.
- •Subjects with normal vital signs.
- •Subjects who agree with patient consent form.
排除标准
- •Subjects with known allergy to the products tested.
- •Smoking more than 10 cigarettes per day and could not tolerate cigarette cessation during each clinical period.
- •Subjects who has used any drug including prescription or Over-The-Counter (OTC) drugs within 7 days prior to the start of the study and might need drug intake during study period.
- •History of alcohol or drug abuse within 2 years before the start of the study.
- •Heavy drinker of caffeine, grapefruit juice or caffeinated drinks or who are on special diet (such as vegetarians) or do exertional physical activity.
- •A history of difficulty with donating blood or donation of more than 500 ml blood within 7 days prior to the start of the study.
研究者
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