NCT01283932已完成1 期
A Randomized, Two-treatment, Two-period, Two-sequence,Single Dose, Crossover Bioequivalence Study of Pantoprazole Sodium 40 mg Delayed Release Tablets (Dr. Reddy's Laboratories Ltd, India) to be Compared With Protonix® 40 mg (Pantoprazole Sodium) Delayed Release Tablets (Wyeth Laboratories, USA) in Healthy, Adult, Human Subjects Under Fed 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
- 52
- 试验地点
- 1
- 主要终点
- Bioequivalence on Cmax and AUC parameters
研究概览
简要总结
To compare the single dose bioavailability of pantoprazole sodium 40 mg delayed release tablets (Dr. Reddy's Laboratories Ltd, India) with Protonix® 40 mg delayed release tablets (Wyeth Laboratories, USA) in 52 (+ 6 standby) healthy, adult, human subjects under fasting conditions.
详细描述
This is a Open label, balanced, randomized two-treatment, two-period,two-sequence, crossover bioequivalence study with at least 07 days washout period between each drug administration under fed conditions.52 (+6 standby) healthy, adult, human subjects were enrolled. A single oral dose of 40 mg of pantoprazole delayed release tablet will be administered along with 240 mL of drinking water within 30 minutes after serving a high fat breakfast.
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 45 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 是
入选标准
- •Subjects will provide written informed consent.
- •Subjects must be healthy human beings within 18-45 years of age (inclusive) weighing at least 50 kg.
- •Subjects must be within ±10% of ideal body weight in relation to height according to Life Insurance Corporation of India height-weight chart for non-medical cases.
- •Subjects must be of normal health as determined by medical history and physical examination performed within 15 days prior to the commencement of the study.
- •Have normal EcG, X-ray and vital signs.
- •Availability of subject for the entire study period and willingness to adhere to protocol requirements as evidenced by written informed consent.
- •If subject is a female volunteer and
- •Is of child bearing potential practicing an acceptable method of birth control for the duration of the study as judged by the investigator(s), such as condoms, foams, jellies, diaphragm, intrauterine device (IUD), or abstinence.
- •is postmenopausal for at least 1 year.
- •is surgically sterile (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy has been performed on the subject)
排除标准
- •Subjects incapable of understanding the informed consent.
- •Subjects with BP≤90/60 or BP≥140/90
- •History of hypersensitivity or idiosyncratic reaction to pantoprazole or other proton pump inhibitors.
- •Any evidence of impairment of renal, hepatic, cardiac, lung or gastrointestinal function.
- •Regular smoker who smokes more than ten cigarettes daily and has difficulty in abstaining from smoking for the duration of each study period.
- •Subjects who has taken over the counter or prescribed medications, including any enzyme modifying drugs or any systemic medication within the past 30 days prior to start of clinical period.
- •History of any psychiatric illness, which may impair the ability to provide written, informed consent.
- •Subjects who have a history of alcohol or substance abuse within the last 5 years.
- •Subjects with clinically significant abnormal values of laboratory parameters.
- •Subjects who have participated in any other clinical investigation using experimental drug or had bled more than 350 mL in the past 3 months.
- •Subjects with positive urine screen for drugs of abuse.
- •Any subject in whom pantoprazole is contraindicated for medical reasons.
- •Female volunteers demonstrating a positive pregnancy screen.
- •Female volunteers who are currently breast-feeding.
研究组 & 干预措施
Pantoprazole Sodium
Experimental
Pantoprazole Sodium DR Tablets 40 mg of Dr. Reddys Laboratories Limited
干预措施: Pantoprazole Sodium (Drug)
Protonix
Active Comparator
Protonix 40 mg DR Tablets of Wyeth Laboratories
干预措施: Pantoprazole Sodium (Drug)
结局指标
主要结局
Bioequivalence 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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