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临床试验/NCT01765023
NCT01765023已完成1 期

An Open-label, Fixed-sequence Study to Evaluate Pharmacokinetic Interactions Between Atorvastatin and Metformin in Healthy Male Subjects

HK inno.N Corporation2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2012年10月最近更新:
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试验速览

阶段
1 期
状态
已完成
入组人数
80
试验地点
2
主要终点
To Evaluate PK interaction of atorvastatin and metformin

研究概览

简要总结

The purpose of the study is to assess the pharmacokinetic interactions between atorvastatin and metformin single or co-administered in healthy volunteers

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
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

入选标准

  • Willing to adhere to protocol requirements and sign a informed consent form
  • Healthy male volunteers who are in age range of 20-55 years and the weight range is not exceed ±20% of ideal weight. Ideal weight = [height -100]*0.9
  • Subjects with no history of any significant chronic disease
  • Judged to be in good health on the basis of their vital sign, ECG, physical exam and routine laboratory data for this trial by investigators

排除标准

  • Subjects taking inducer or inhibitor of drug metabolism enzyme such as barbital within 28days prior to study medication dosing
  • Subjects with Symptoms of acute disease within 28days prior to study medication dosing
  • Subjects with a history of gastrointestinal diseases which might significantly change ADME of medicines
  • Subjects with a history of abdominal surgery within food and water limit
  • Subjects with a history of clinically significant allergies including drug allergies
  • Subjects with anaphylaxis to atorvastatin and/or metformin
  • Subjects with a history or plan iodine radiotherapy within 28 days prior to drug administration
  • Subjects with a history of myopathy
  • Subjects with a hereditary problems, for example, galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
  • Clinical laboratory test values are outside the accepted normal range
  • AST or ALT >1.25 times to normal range
  • Total bilirubin >1.5 times to normal range
  • Creatinine clearance <90 mL/min
  • Subjects with a history of drug, caffeine and alcohol abuse(caffeine > 5cups/day, cigarette > 10/day, alcohol > 30g/day) or have ever drank within 7 days prior to drug administration
  • Special diet known to interfere with the absorption, distribution, metabolism or excretion of drugs (especially, consumption of grapefruit juice) within 7 days prior to drug administration
  • Donated blood within 60 days prior to dosing
  • Participated in a previous clinical trial within 60 days prior to dosing
  • Subjects who have received any drugs that might confound the results of the trial based on medical judgement by investigators within 10days prior to drug administration
  • Subjects considered as unsuitable based on medical judgement by investigators

结局指标

主要结局

To Evaluate PK interaction of atorvastatin and metformin

时间窗: Throughout the study

次要结局

  • To Evaluate PK interaction of 2-OH-atorvastatin and metformin(Throughout the study)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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