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临床试验/KCT0000999
KCT0000999已完成未知

Open Label, Randomized, Crossover Study to Evaluate a Pharmacokinetic Drug Interaction Between Lobeglitazone and Warfarin in Healthy Subjects

Chong Kun Dang0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 55(Year)(—)
性别
Male

入选标准

  • 1) A healthy male volunteer between 19 and 55 years old.
  • 2) BMI between 19 and 27.
  • 3) Signed the informed consent form prior to study participation.
  • 4) Able to participate in the entire trial

排除标准

  • 1) Clinically significant hepatic, renal, digestive system, respiratory system, endocrine system, nervous system, hematologic, cardiovascular system, tumor or have history of tumor
  • 2) Clinically significant hemorrhagic disease
  • 3) Genetic problems such as galactose intolerance, Lapp lactase deficiency, glucose-galactose malabsorption
  • 4) Have hypersensitivity reactions history for lobeglitazone, warfarin, excipient of IP or aspirin, antibiotics
  • 5) Medication which might significantly alter the absorption, distribution, metabolism, or excretion of investigational products within 30 days prior to screening
  • 6) Participated in the other clinical trials and administrated IP within 60 days prior to screening
  • 7) Subject takes ethical drug or herbal medicine within 14 days, OTC within 7 days before screening
  • 8) Previously donate whole blood within 60 days or component blood within 30 days
  • 9) sit SBP < 90mmHg or sit SBP = 140mmHg or sit DBP < 60mmHg or sit DBP = 90mmHg
  • 10) A heavy alcohol consumer (alcohol > 140 g/week) or cannot stop drinking
  • 11) A heavy smoker (cigarette > 10 cigarettes per day) or cannot stop smoking
  • 12) A heavy caffeine consumer (more than 4cups per a day) or A heavy grapefruit consumer (more than 1cup per a day) or cannot stop having
  • 13)Positive for the Triage TOX drug on urine
  • 14) Positive for HIV antibody, HBsAg, HCV antibody test
  • 15) AST, ALT or Total bilirubin > UNL * 1.5
  • 16) Estimated GFR < normal limit
  • 17) INR, aPTT over the normal limit
  • 18) Clinically significant laboratory test result
  • 19) Clinically significant ECG
  • 20) An impossible one who participates in clinical trial by investigator's decision including other reason

研究者

发起方
Chong Kun Dang

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