Comparative bioequivalence study of ASAVER® 81 mg Enteric-coated Tablet of Actoverco. and Aspirin Bayer® of BAYER as reference 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: 2022年8月29日

试验速览

暂无简介。

•Healthy subjects (male) between 20 – 45 years of age and Body Mass Index (BMI) within 15% of normal range between 18.5 - 30 kg/m2.
•Subjects with no significant diseases or clinically significant abnormal findings during screening, medical history, clinical examination and laboratory evaluations.
•Subjects that have normal vital signs.
•Subjects who agree with patient consent form.

•Hypersensitivity to the ASA, other NSAIDs and/or to inactive constituents.
•Smoking more than 10 cigarettes per day and could not tolerate cigarette cessation during each clinical period.
•Taking citrus fruits or their juices within 5 days before initiation of the study;
•Any vaccination within 28 days and administration of any biologics within 4 months before initiation of the study.
•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.

发起方

Actover Pharmaceutical Co.