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临床试验/NL-OMON36726
NL-OMON36726已完成不适用

A One-Way Drug-Drug Interaction Study to Assess the Effect of Ritonavir-boosted Atazanavir on the Pharmacokinetics, Safety and Tolerability of BMS-790052 in Healthy Subjects - BMS-790052/ritonavir-boosted atazanavir drug-drug interaction study

Bristol-Myers Squibb0 个研究点目标入组 14 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
14

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 4 weeks after last dose of study medication

排除标准

  • - Any significant acute or chronic medical illness.
  • - 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.
  • - Recent (within 6 months of study drug administration) drug or alcohol abuse as defined in DSM IV, Diagnostic Criteria for Drug and Alcohol Abuse (see Appendix 1).
  • - History of cardiac conduction abnormalities.
  • - History of nephrolithiasis.
  • - 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, HIV viral load, or HIV-1, -2 antibody
  • - History of any significant drug allergy (such as Stevens-Johnson Syndrome, anaphylaxis or hepatotoxicity).
  • - 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)

研究者

发起方
Bristol-Myers Squibb

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