NCT01131780已完成1 期
A Randomized, Open Label, 2-treatment, Single Dose, Crossover, Bioequivalence Study of Ibuprofen 200 mg+Pseudoephedrine HCL 30 mg Tablets of Dr. Reddy's and Advil® Cold and Sinus Caplets of Wyeth Consumer Healthcare Under Fasting Conditions.
适应症
干预措施
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 32
- 试验地点
- 1
- 主要终点
- Bioequivalence based on Cmax and AUC parameters
研究概览
简要总结
The purpose of this study is to assess the bioequivalence of Ibuprofen 200 mg + Pseudoephedrine HCL 30 mg under fasting conditions.
详细描述
This study assess the bioequivalence of Ibuprofen 200 mg + Pseudoephedrine HCL 30 mg Tablets of Dr. Reddy's and Advil® Cold and Sinus Caplets of Wyeth Consumer Healthcare in healthy human adult subjects with the single oral administration under fasting conditions with a washout period of 7 days.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Healthy human subjects between 18-50 years of age (inclusive), weighing as per the standard height and weight chart of Life Insurance Corporation of India (II Underweight and Overweight Min. & Max. Chart)
- •Subjects who have no evidence of underlying disease during screening medical history and whose physical examination is performed within 21 days to commencement of the study.
- •Subjects whose screening laboratory values are within normal limits or considered by the physician/Principal Investigator to be of no clinical significance.
- •Informed consent given in written form according to section 10.3 of the protocol.
- •Female Subjects:
- •of child bearing potential practicing an acceptable method of birth control for the duration of study as judged by the investigator(s), such as condoms, foams, jellies, diaphragm, intrauterine device (IUD), or abstinence.
- •postmenopausal for at least 1 year.
- •surgically sterile (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy has been performed on the subject.
排除标准
- •History or presence of significant:
- •Cardiovascular, pulmonary, hepatic, renal hematological; gastrointestinal, endocrine, immunologic, dermatologic, musculoskeletal, neurological or psychiatric disease.
- •Alcohol dependence, alcohol abuse or drug abuse within past one year.
- •Moderate to heavy smoking (> 10 cigarettes/day) or on assumption of tobacco products.
- •History of difficulty in swallowing.
- •Clinically significant illness within 4 weeks before the start of the study
- •Asthma, urticaria or other allergic type reactions after taking any medication.
- •Subjects who, through completion of the study, would have donated in excess of:
- •500ml of blood in 14 days, or
- •500 - 800 m l of blood in 14 days (unless approved by the Principal Investigator)
- •1000 ml of blood in 90 days
- •1250 ml of blood in 120 days
- •1500 ml of blood in 180 days
- •2000 ml of blood in 270 days
- •2500 ml of blood in 1 year
- •Participation in another clinical trial within the preceding 28 days of study start.
- •Subjects who have:
- •Systolic blood pressure less than 90 mm of Hg and more than 150 mm of Hg
- •Diastolic blood pressure less than 60 m of Hg and more than 95 mm of Hg. Minor deviations (1-3 mm Hg) at check-in may be acceptable at the discretion of the physician/investigator
- •Pulse rate below 50/min. and above 105/min.
- •Female volunteers demonstrating a positive pregnancy screen or currently breast-feeding.
研究组 & 干预措施
Ibuprofen + Psuedoephedrine Hydrochloride
Experimental
Ibuprofen 200 mg + Pseudoephedrine HCL 30 mg Tablets
干预措施: Ibuprofen + Pseudoephedrine Hydrochloride (Drug)
Advil® Cold and Sinus
Active Comparator
Advil® Cold and Sinus Tablets of Wyeth Consumer Healthcare
干预措施: Ibuprofen + Pseudoephedrine Hydrochloride (Drug)
结局指标
主要结局
Bioequivalence based on Cmax and AUC parameters
时间窗: 2 months
次要结局
未报告次要终点
研究者
研究点 (1)
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