A Safety And Pharmacokinetic Study of Setrobuvir Alone and In Combination With Ritonavir-Boosted Danoprevir in Subjects With Mild Hepatic Impairment Compared to Healthy Controls
A Multi Center, Sequential, Open-Label, Multiple-Dose Study of Setrobuvir (STV) Alone and With Co-Administration of Ritonavir-boosted Danoprevir to Evaluate the Safety, Tolerability and Pharmacokinetics of STV, DNV, and Ritonavir (RTV) in Subjects With Mild Hepatic Impairment Compared to Healthy Controls
研究概览
研究类型
注册 (实际的)
阶段
- 阶段1
联系人和位置
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Male and female adults, 18-65 years of age, inclusive
- Weight >/= 45.0 kg
- Body mass index (BMI) 18.0 - 35.0 kg/m2, inclusive
- Females of childbearing potential and males and their female partners of childbearing potential must agree to use two forms of non-hormonal contraception as defined by protocol
- Subjects with a history of substance abuse may be enrolled provided they have not abused drugs or alcohol for at least 6 months
- Healthy subjects only:
Medical history without major recent or ongoing pathology Laboratory values at screening and Day -1 within the normal range or showing no clinically relevant deviations
- Subjects with hepatic impairment only:
Stable mild liver disease (Child-Pugh A) of cryptogenic, post-hepatic, hepatitis B/C, or alcoholic origin Stable hepatic impairment defined as no clinically significant change in disease status within the last 30 days Must be on stable dose of medication and/or treatment regimen at least 2 weeks before dosing of study medication
Exclusion Criteria:
- Pregnant or lactating women or males with female partners who are pregnant or lactating
- Active infection or febrile illness </= 10 days prior to the first dose of study medication
- Uncontrolled/untreated hypertension
- Inadequate renal function
- Positive urine drug screen or positive breath alcohol test at screening and on Day -1 of each period
- An average alcohol intake of more than 2 units per day or 14 units per week until 48 hours prior to enrollment
- History of any significant drug-related allergy or hepatotoxicity
- Participation in other clinical studies with an investigational drug or new chemical entity within 3 months (6 months for biologic therapies) prior to the first dose of study medication
- Positive for HIV infection
- Any clinically significant cardiovascular or cerebrovascular disease
- Healthy subjects only:
Any clinically significant concomitant disease or condition that could interfere with, or for which the treatment might interfere with, the conduct of the study, absorption of medication, or that would, in the opinion of the investigator, pose an unacceptable risk to the subject in this study Positive screening test for HBsAg or HCV antibody
- Subjects with hepatic impairment only:
Severe ascites at screening or Day -1 History of or current severe hepatic encephalopathy (Grade 3 or higher) Biliary liver cirrhosis or other causes of hepatic impairment not related to parenchymal disorder and/or disease of the liver Positive screening test for HCV antigen
学习计划
研究是如何设计的?
设计细节
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:A: setrobuvir
|
200 mg orally every 12 hours
|
|
实验性的:B: setrobuvir + DNV/r
|
200 mg orally every 12 hours
100 mg orally every 12 hours
100 mg orally every 12 hours
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Safety: Incidence of adverse events
大体时间:approximately 40 days
|
approximately 40 days
|
|
Pharmacokinetics: Maximum plasma concentration at steady-state (Css,max)
大体时间:up to 16 days
|
up to 16 days
|
|
Pharmacokinetics: Total area under the concentration-time curve form time 0 to 12 hours post-dose at steady-state (AUCss,0-12h)
大体时间:up to 16 days
|
up to 16 days
|
|
Pharmacokinetics: Plasma concentration at steady-state 12 hours post-dose (Css, 12h)
大体时间:up to 16 days
|
up to 16 days
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Pharmacokinetics: Time to maximum plasma concentration (tmax)
大体时间:up to 16 days
|
up to 16 days
|
|
Pharmacokinetics: Elimination half-life (t1/2)
大体时间:up to 16 days
|
up to 16 days
|
|
Pharmacokinetics: Apparent oral clearance at steady-state (CLss/F)
大体时间:up to 16 days
|
up to 16 days
|
|
Pharmacokinetics: Cumulative amount excreted at steady-state (Aess)
大体时间:up to 16 days
|
up to 16 days
|
|
Pharmacokinetics: Fraction of orally administered drug excreted into urine (fe/f)
大体时间:up to 16 days
|
up to 16 days
|
|
Pharmacokinetics of danoprevir in combination with setrobuvir: Area under the concentration-time curve (AUC)
大体时间:up to 12 days
|
up to 12 days
|
|
Pharmacokinetics of ritonavir in combination with setrobuvir: Area under the concentration-time curve (AUC)
大体时间:up to 12 days
|
up to 12 days
|
合作者和调查者
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- NP28326
- 2012-002283-28 (EudraCT编号)
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