An Open-label, Randomized, Single-dose, 2-way Crossover Trial to Compare the Pharmacokinetics of Repaglinide2mg and MetforminHCl 500mg Complex to Combination Preparation of Repaglinide 2mg and MetforminHCl 500mg in Healthy Male Volunteers.
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 48
- 试验地点
- 1
- 主要终点
- AUCt and Cmax of repaglinide and metformin
研究概览
简要总结
This is a phase-1, single center, open-label, randomized, single-dose, 2-way crossover study. The objective of the study is to compare the pharmacokinetic properties after co-administration of Repaglinide 2mg and Metformin hydrochloride 500mg with administration of combination preparation of Repaglinide 2mg and Metformin hydrochloride 500mg in 50 healthy male volunteers.
详细描述
This is a phase-1, single center, open-label, randomized, single-dose, 2-way crossover study. The objective of the study is to compare the pharmacokinetic properties after co-administration of Repaglinide 2mg and Metformin hydrochloride 500mg with administration of combination preparation of Repaglinide 2mg and Metformin hydrochloride 500mg in 50 healthy male volunteers.
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All the subjects should be admitted one day prior to scheduled study date until 4pm to Chonbuk National University Hospital Clinical Trial Center and they will be served with the same dinner. After dinner, they should keep fast, they are just allowed to drink water until 8am of the study date.
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According to the randomly designated order, all subjects will be administrated with the study or reference products with 240mL of water at 9am(±2hours) on the first date of the study. The study or the reference products should be swallowed completely, and not to be chewed before swallowing.
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Study product : Repanorm M 2/500mg (Dalim BioTech Co., Ltd.)
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Reference products : Metformin HCl 500mg tablet, Repaglinide 2mg tablet
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Subjects have to fast for 4 hours post administration of the study or reference drugs(water intake is not allowed for 1 hour before and after the administration), and should follow standardized lunch after four hours and dinner 9 hours later from the time of administration
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
- 20 Years 至 55 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 是
入选标准
- •Healthy male volunteers ages between 20 and 55 years at screening
- •Subject with Body Mass Index(BMI) with the range of 17.5 to 30.5kg/m2 and body weight over 45kg
- •Signed informed consent with the date of signature
- •With ability to comply with all the scheduled visits, treatment plans; laboratory tests and other processes.
排除标准
- •Positive of blood, kidney, endocrine, lung, gastro-intestinal, cardiovascular, hepatic, psychiatric, nervous, allergy; or with past and present disease history or symptoms that are clinically significant.
- •Any conditions that are likely to affect drug absorption. ex) gastrectomy
- •Positive on urine drug tests
- •History of drinking alcohol more than 12 ounces(360mL) of beer, 1.5 ounces(45mL) of liquor; or 21 drinks/week(1drink = 5 ounces(150mL) of wine ) 6months prior to screening
- •Participation in any other clinical studies within 2months prior to scheduled study drug administration
- •With Blood pressure of ≥ 160 mmHg(Systolic blood pressure) or ≥ 90 mmHg(Diastolic blood pressure) in sitting position at screening time.
- •History of any serious substance or alcohol abuse within one year prior to screening
- •Use of any drugs known to significantly induce or inhibit drug metabolizing enzyme within 30days prior to scheduled study drug administration
- •Cigarette smoking of over 20 sticks per day.
- •Use of any prescription drugs or any over the counter drugs within 10days or quintuple half life(whichever is longer) prior to scheduled study drug administration
- •Donation of whole blood within 2months or any blood products within 1month, prior to scheduled study drug administration
- •Disability to comply with the guidelines written on the protocol
- •Severe acute/chronic medical, physical disorder or laboratory test abnormality that are likely to alter the study result and increase the risk by participating in the study and study drug administration
- •Hypersensitivity to chief component or excipient of Repaglinide
- •History of hypersensitivity to Metformin or Biguanide class of drugs
- •With renal failure or renal inadequacy caused by cardiovascular shock, acute myocardial infarction and sepsis
- •With Congestive heart failure and undergoing drug treatment.
- •Patients undergoing radioactive iodine uptake tests, such as intravenous urography, intravenous cholangiography, angiography, computed tomography using radioactive iodine
- •Patients with type 1 diabetes, acute or chronic metabolic acidosis including diabetic ketoacidosis associated with or without coma
- •With serious infection or trauma
- •Malnutrition, starvation; weakness; pituitary insufficiency or adrenal insufficiency
- •Patients with hepatic failure, pulmonary infarction, serious pulmonary dysfunction, or other conditions associated with hypoxemia, alcohol abuser, or dehydration, diarrhea; vomiting and gastro-intestinal disease
- •Proven to be unsuitable to participate in this clinical study by an investigator
研究组 & 干预措施
Sequence A
干预措施: Repaglinide/Metformin combination, Repaglinide, Metformin (Drug)
Sequence B
干预措施: Repaglinide/Metformin combination, Repaglinide, Metformin (Drug)
结局指标
主要结局
AUCt and Cmax of repaglinide and metformin
时间窗: Before study drug administration(0h) and after 0.25h, 0.5h, 0.75h, 1h, 1.5h, 2h, 2.5h, 3h, 4h, 6h, 8h, 12h, 24h of study drug administration.
次要结局
- AUC∞, Tmax, t1/2, CL/F and Vd/F of repaglinide and metformin(Before study drug administration(0h) and after 0.25h, 0.5h, 0.75h, 1h, 1.5h, 2h, 2.5h, 3h, 4h, 6h, 8h, 12h, 24h of study drug administration.)