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临床试验/SLCTR/2017/035
SLCTR/2017/035尚未招募4 期

A Bioequivalence study on the innovator and a generic amoxicillin trihydrate 500mg capsules in healthy volunteers

niversity of Colombo0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Healthy volunteer males and females of 18-55 years of age.
  • 2. Weight within the normal range according to accepted normal values for the Body Mass Index between 18-25 kg/m2
  • 3. Stable health screening for medical and medical histories, physical examination, vital signs, ECG, Renal Function Test, Liver Function Test, Blood Glucose, Complete Blood Count and urine pregnancy test for females.
  • 4. Preferably be non-smokers and without a history of alcohol or drug abuse.

排除标准

  • 1. History of allergic reactions to the selected drug and or its constituents
  • 2. History or concurrent symptoms of allergy, cardiovascular, liver, kidney, gastrointestinal, hematological disorders and/or any disease that may affect the bioavailability of the drug
  • 3. Regular alcohol consumption (more than 1 time/week) or drug abuse
  • 4. Smokers or ex-smoker less than 30 days
  • 5. Use of any drugs within 14 days prior to administration of the first study drug and willing to take them throughout the study period
  • 6. Use of food supplements taken as capsules or tablets or neutraceuticals, vitamins, minerals, herbal remedies, and/or contraceptives hormonal within 14 days before first study drug administration and willing to taking them throughout the study period
  • 7. History of gastrointestinal disease
  • 8. Already participated in another clinical study within last 30 days
  • 9. Pregnant (positive pregnancy test) or breast feeding
  • 10. Blood donation within last 90 days

研究者

发起方
niversity of Colombo

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