IRCT20180620040164N4已完成未知
Randomized, single-dose, crossover comparative bioequivalence study of Linagliptin 5 mg tablets of Alhavi pharmaceutical co. and Boehringer in 24 healthy male under fasting conditions
Alhavi 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
- 18 years 至 45 years(—)
- 性别
- Male
入选标准
- •Healthy subjects (male) between 18 – 45 years of age and Body Mass Index (BMI) 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 ECG and vital signs.
- •Subjects who agree with patient consent form.
排除标准
- •Known hypersensitivity to linagliptin or inactive ingredients
- •Acute and chronic cardiovascular, respiratory, gastrointestinal diseases, neuroendocrine disorders, blood system disorders and renal or hepatic impairment
- •Acute infectious diseases less than 1 weeks prior to the start of the study
- •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 14 days prior to the start of the study and might need drug intake during study period
- •Subjects who have a history of alcohol or substance abuse within the last 5 years
- •Heavy drinker of alcohol, 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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