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临床试验/NCT01089166
NCT01089166已完成1 期

To Compare the Bioavailability of Extended Release Metformin HCl Tablet(Test Formulation, Torrent Pharmaceuticals Ltd.,India) Versus Glucophage XR® Tablets ( Reference Formulation, Bristol-Myers Squibb Company, USA) in Healthy Human Volunteers Under Fasting Condition

Torrent Pharmaceuticals Limited1 个研究点 分布在 1 个国家开始时间: 2010年3月18日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
试验地点
1

研究概览

简要总结

Objective: To compare the bioavailability of Extended Release Metformin HCl Tablet(Test formulation, Torrent Pharmaceuticals Ltd.,India) versus Glucophage XR® Tablets ( Reference formulation, Bristol-Myers Squibb Company, USA) in Healthy Human Volunteers under fasting condition.

Study Design: An Open-Label, Randomised, 2-Period, 2-Treatment,Crossover Study under fasting condition.

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Subjects must meet all of the following criteria in order to be included in the study:
  • Age: 18 - 45 years.
  • Subject with BMI of 18-27 (inclusive both) kg/m2 with minimum of 50 kg weight.
  • Healthy and willing to participate in the study.
  • Subject willing to adhere to the protocol requirements and to provide written informed consent.
  • Non-smokers or smoker who smokes less than 10 cigarettes a day.

排除标准

  • The subjects will be excluded from the study based on the following criteria:
  • Clinically relevant abnormalities in the results of the laboratory screening evaluation.
  • Clinically significant abnormal ECG or Chest X-ray.
  • Systolic blood pressure less than 100 mm Hg or more than 140 mm Hg and diastolic blood pressure less than 60 mm Hg or more than 90 mm Hg.
  • Pulse rate less than 50/minute or more than 100/minute.
  • Oral temperature less than 95°F or more than 98.6°F.
  • Respiratory rate less than 12/minute or more than 20/minute
  • Addiction to alcohol or history of any drug abuse within the past 2 years.
  • Recent History of kidney or liver dysfunction.
  • History of allergy to the test drug or any drug chemically similar to the drug under investigation.
  • Administration/ Intake of prescription or OTC medication for two weeks before the study.
  • Patients suffering from any chronic illness such as arthritis, asthma etc.
  • HIV, HCV, HBsAg positive Subjects.
  • Opioids, tetra hydrocannabinoids, amphetamine, barbiturates, benzodiazepine, Cocaine positive Subjects based on urine test.
  • Subjects suffering from any psychiatric (acute or chronic) illness requiring medications.
  • Administration of any investigational products in the period 0 to 3 months before entry to the study.
  • Intake of barbiturates or any enzyme-inducing drug in last three months.
  • History of significant blood loss due to any reason, including blood donation in the past 12 weeks. The total blood loss in last 3 months including for this study will not exceed 350ml.
  • History of any bleeding disorder.
  • Existence of any surgical or medical condition, which, in the judgement of the Chief investigator and/or clinical investigator, might interfere with the absorption, distribution, metabolism or excretion of the drug or likely to compromise the safety of Subjects.
  • Inability to communicate or co-operate due to language problem, poor mental development or impaired cerebral function.

研究组 & 干预措施

Torrent's Metformin tablets 500 mg

Experimental

干预措施: Metformin (Drug)

Glucophage XR® of Bristol- Myers Squibb Company, USA)

Active Comparator

干预措施: Metformin (Drug)

研究者

申办方类型
Industry

研究点 (1)

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