跳至主要内容
临床试验/NL-OMON36725
NL-OMON36725已完成不适用

An Open-Label Two-Way Drug-Drug Interaction Study to Assess the Effect of Tenofovir on the Pharmacokinetics of BMS-790052 and the Effect of BMS-790052 on the Pharmacokinetics of Tenofovir in Healthy Subjects - BMS-790052/tenofovir drug-drug interaction study

Bristol-Myers Squibb0 个研究点目标入组 21 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
21

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

年龄范围
18 至 99(—)

入选标准

  • Age: 18-49 years, inclusive
  • BMI: 18.0 - 32.0 kg/m2, inclusive
  • Women of child bearing potential should use adequate contraception (e.g., double barrier method) until at least 12 weeks after last dose of study medication

排除标准

  • - Any significant acute or chronic medical illness (especially renal disease).
  • - Current or recent (within 3 months of study drug administration) gastrointestinal disease indicated as clinically relevant by the Medical Investigator.
  • - Any major surgery within 4 weeks of study drug administration.
  • - Any gastrointestinal surgery that could impact upon the absorption of study drug.
  • - Donation of blood or plasma to a blood bank or in a clinical study (except a screening visit) within 90 days of study drug administration.
  • - Blood transfusion within 90 days of study drug administration.
  • - Inability to tolerate oral medication.
  • - Inability to swallow oral medication in the form of tablets or capsules.
  • - Inability to be venipunctured and/or tolerate venous access.
  • - Smoking more than 5 cigarettes per day.
  • - History of renal disease including but not limited to acute renal failure and Fanconi syndrome.
  • - History of pathologic fracture or other significant risk factors for osteoporosis or bone loss.
  • - Recent (within 6 months of study drug administration) drug or alcohol abuse
  • - Any other sound medical, psychiatric and/or social reason as determined by the investigator.
  • - Evidence of organ dysfunction or any clinically significant deviation from normal in physical examination, vital signs, ECG or clinical laboratory determinations beyond what is consistent with the target population.
  • - Positive urine screen for drugs of abuse.
  • - Positive blood screen for hepatitis C antibody, hepatitis B surface antigen (HBsAg), HIV viral load or HIV-1, -2 antibody
  • - Serum creatinine > upper limit of normal (ULN).
  • - History of any significant drug allergy (such as anaphylaxis, hepatotoxicity or rash).
  • - Pregnancy or lactation (females only).
  • - Prisoners or subjects who are involuntarily incarcerated.
  • - Subjects who are compulsorily detained for treatment of either a psychiatric or physical (eg, infectious disease) illness

研究者

发起方
Bristol-Myers Squibb

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