Comparative bioequivalence study of Ciprofloxacine 500 mg Tablet of Cosar Pharmaceutical Co. and Ciprobay 500 mg tablet of BAYER as reference in 24 healthy male under fasting.

Cosar Pharmaceutical Co.0 个研究点目标入组 24 人开始时间: 待定最近更新: 2024年6月24日

试验速览

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•Healthy subjects (male) between 18 – 50 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.
•ubjects that have normal vital signs.
•Subjects who agree with patient consent form.

•Previous history of allergy to a fluoroquinolone or severe allergic reaction to any medication.
•History of CNS disorders (e.g. convulsive seizures).
•History or presence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, neuromuscular, psychiatric, auto-immune or neurological disorders.
•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.
•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

Cosar Pharmaceutical Co.