NCT01270308已完成1 期
Open Label, Randomized, Two-treatment, Three-period, Three-sequence, Partial Replicate Oral Bioequivalence Study of Lansoprazole 30 mg DR Capsules of Dr.Reddy's Laboratories Limited, India Comparing With That of PREVACID® (Containing Lansoprazole) 30 mg DR Capsules of TAP Pharmaceuticals Inc. USA, in Healthy, Adult, Human Subjects 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
- 48
- 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 objective of this study was to compare the relative bioavailability of Lansoprazole DR Capsules 30 mg with Prevacid® Capsules 30 mg under fasting conditions in healthy adult human subjects.
详细描述
open label, randomized, two-treatment, three-period, three-sequence, partial replicate oral bioequivalence study of Lansoprazole 30 mg DR Capsules of Dr.Reddy's Laboratories Limited, India comparing with that of PREVACID® (containing Lansoprazole) 30 mg DR Capsules of TAP Pharmaceuticals Inc. USA, in healthy, adult, human subjects under fasting conditions. 48 healthy, adult, human subjects were enrolled in the study and 42 subjects were completed the study.
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
- All
- 接受健康志愿者
- 是
入选标准
- •i. Provided written informed consent.
- •ii. Subject who were healthy, adult, human beings within 18 and 45 years of age (both inclusive) weighing at least 50 kg.
- •iii. Subject having a body mass index between 18.0 and 29.9 (both inclusive), calculated as weight in Kg/height in m
- •iv. Subject having a normal health as determined by medical history, physical examination and laboratory investigation performed within 28 days prior to the commencement of the study. (Laboratory values must be within normal limits or considered by the physician /investigator to be of no clinical significance).
- •v. Female Subjects 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.
- •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
- •i. Subject who were incapable of understanding the informed consent.
- •ii. Systolic blood pressure less than 90 mm of Hg or more than 140 mm of Hg.
- •iii. Diastolic blood pressure less than 60 mm of Hg or more than 90 mm of Hg.
- •iv. Oral temperature is below 95.0°F or above 98.6°F.
- •v. Pulse rate below 50/min or above 100/min.
- •vi. History of hypersensitivity or idiosyncratic reaction to investigational drug product or any other related drugs.
- •vii. Any evidence of impairment of renal, hepatic, cardiac, lung or gastrointestinal function.
- •viii. Consumption of grapefruit for the past ten days prior to the check-in, in each period.
- •ix. Regular smoker who has a habit of smoking more than nine cigarettes per day and has difficulty in abstaining from smoking during sample collection period.
- •x. Habit of alcoholism and difficulty in abstaining from alcohol during the sample collection period.
- •xi. Difficulty in abstaining from xanthene containing food or beverages (like tea, coffee, chocolates and cola drinks) during the sample collection period.
- •xii. Intake of over the counter (OTC) or prescribed medications and enzyme modifying medication or systemic medication for the last 30 days before dosing.
- •xiii. Clinically significant abnormalities and / or with significant diseases.
- •xiv. Confirmed positive in alcohol screening.
- •xv. Confirmed positive in selected drug of abuse.
- •xvi. Subjects who had participated in any other clinical investigation using experimental drug/donated blood in past 90 days before the date of start of study
- •xvii. Confirmed positive in urine pregnancy test.
- •xviii. Female detected to be pregnant, breast feeding or who is likely to become pregnant during the study.
研究组 & 干预措施
Lansoprazole DR Capsules 30 mg
Experimental
Lansoprazole DR Capsules 30 mg of Dr.Reddy's Laboratories Limited
干预措施: Lansoprazole (Drug)
Prevacid 30 mg Capsules
Active Comparator
Prevacid 30 mg Capsules of TAP Pharmaceuticals Inc. USA
干预措施: Lansoprazole (Drug)
结局指标
主要结局
Bioequivalence based on Cmax and AUC parameters
时间窗: 4 months
次要结局
未报告次要终点
研究者
研究点 (1)
Loading locations...
相似试验
已完成
1 期
Lansoprazole 30 mg DR Capsule Fasting StudyHealthyNCT01045967Teva Pharmaceuticals USA56
已完成
1 期
Lansoprazole 30 mg DR Capsule Replicate Food StudyHealthyNCT01046084Teva Pharmaceuticals USA50
已完成
1 期
Lansoprazole 30 mg DR Capsule Fasting Replicate Sprinkle StudyHealthyNCT01046253Teva Pharmaceuticals USA50
已完成
1 期
PK-PD Comparative Study of Lansoprazole Capsules and Lansoprazole Enteric-coated Capsules in Healthy Chinese VolunteersEffect of DrugsSafety IssuesNCT03488186First Affiliated Hospital of Zhejiang University24
已完成
1 期
Study to Investigate the Relative Bioavailability, Influence of Pantoprazole Coadministration and Food Effect of Different Oral Formulation of BI 113608HealthyNCT01703858Boehringer Ingelheim15