Individualized Triple-therapy Using Boceprevir in HIV-positive Patients With Hepatitis C (HIVCOBOC-RGT)
Response-guided Triple-therapy Using Boceprevir in Combination With PEGIFN/RBV in HIV/HCV-coinfected Patients
Response-guided triple-therapy with boceprevir (BOC) in combination with pegylated interferon (PEGIFN) and ribavirin (RBV) is the current standard of care for HIV-negative patients infected with hepatitis C genotype (HCV-GT) 1. In contrast, in HIV-positive patients, a fixed treatment duration of 48 weeks is used.
The aim of this study is to assess efficacy and safety of response-guided triple-therapy with BOC in combination with PEGIFN and RBV in HIV-positive patients. Thus, treatment duration will be individualized based on HCV-RNA negativity at treatment week 8 (W8). All patients will receive 4 weeks of PEGIFN/RBV lead-in. Patients with undetectable HCV-RNA at W8 will be treated with 24 weeks of BOC/PEGIFN/RBV triple-therapy resulting in a total treatment duration of 28 weeks, while patients with detectable HCV-RNA at W8 will receive 44 weeks of BOC/PEGIFN/RBV triple-therapy and a total treatment duration of 48 weeks.
研究概览
研究类型
注册 (实际的)
阶段
- 第四阶段
联系人和位置
学习地点
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Vienna、奥地利、1090
- Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna
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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:
- Confirmed HIV infection (anti-HIV1/2 antibody positive).
- Chronic HCV infection (anti-HCV positive, HCV-RNA detectable for >6 months).
- HCV-GT 1 infection.
- Age ≥18 years and ≤65 years.
- No prior treatment with BOC/PEGIFN/RBV.
- CD4+ cell count >200 cells/µL.
- Stable antiretroviral therapy (ART) including tenofovir/emtricitabine (Truvada®, Gilead) and raltegravir (Isentress®, MSD) with HIV-RNA <50 copies/mL.
- Valid result on transient elastography or liver biopsy within 6 months prior to enrollment.
- Female patients of childbearing potential must agree to use an effective contraceptive during treatment and for 4 months after treatment has been concluded.
- Male patients or their female partners must agree to use an effective contraceptive during treatment and for 7 months after treatment has been concluded.
Exclusion Criteria:
- HCV-GT other than HCV-GT 1.
- Cirrhotic patients (as defined by METAVIR F4 in liver biopsy or liver stiffness >12.3 kPa) with decompensated liver disease (Child-Pugh stage B/C).
- Chronic liver diseases other than hepatitis C virus infection (hepatitis B virus infection: HBsAg positivity, nonalcoholic steatohepatitis, autoimmune hepatitis, primary biliary cirrhosis, hemochromatosis, Wilson's disease, alpha-1 antitrypsin deficiency, cystic fibrosis).
- Significant cardiac disease (ejection fraction <40% at echocardiography).
- Significant pulmonary disease (COPD stage GOLD III/IV).
- Significant renal disease (serum creatinine >1.5 mg/dL).
- Subjects taking medication(s) that is/are highly dependent on CYP3A4/5 for clearance, and for which elevated plasma concentrations are associated with serious and/or life-threatening events such as but not limited to, orally administered midazolam, pimozide, amiodarone, flecainide, propafenone, quinidine, and ergot derivatives (dihydroergotamine, ergonovine, ergotamine, methylergonovine).
- Contraindications for boceprevir (Victrelis®, MSD), pegylated interferon alpha-2a (Pegasys®, Roche) or ribavirin (Copegus®, Roche), as listed in section 4.3 of the respective summary of product characteristics (SmPCs).
- Ongoing alcohol abuse (average daily alcohol consumption >50g).
- Ongoing illicit drug abuse.
- Unwillingness to give written informed consent.
- Pregnancy and breastfeeding.
- Women wishing to become pregnant.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:28 weeks of treatment duration
All patients will receive 4 weeks of PEGIFN/RBV lead-in.
Patients with undetectable HCV-RNA at treatment week 8 will be treated with 24 weeks of BOC/PEGIFN/RBV triple-therapy resulting in a total treatment duration of 28 weeks.
|
180mcg once weekly; subcutaneous injection
其他名称:
600mg two times daily (BID) (e.g.
3x200mg at 6am, 3x200mg at 6pm) in patients ≥75kg body weight; 2x200mg at 6am and 3x200mg at 6pm in patients <75kg; orally
其他名称:
800mg three times daily (TID) (e.g.
4x200mg at 6am, 4x200mg at 2pm, 4x200mg at 10pm); orally
其他名称:
|
|
实验性的:48 weeks of treatment duration
All patients will receive 4 weeks of PEGIFN/RBV lead-in.
Patients with detectable HCV-RNA at treatment week 8 will receive 44 weeks of BOC/PEGIFN/RBV triple-therapy and a total treatment duration of 48 weeks
|
180mcg once weekly; subcutaneous injection
其他名称:
600mg two times daily (BID) (e.g.
3x200mg at 6am, 3x200mg at 6pm) in patients ≥75kg body weight; 2x200mg at 6am and 3x200mg at 6pm in patients <75kg; orally
其他名称:
800mg three times daily (TID) (e.g.
4x200mg at 6am, 4x200mg at 2pm, 4x200mg at 10pm); orally
其他名称:
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Proportion of Subjects With Sustained Virologic Response (SVR12)
大体时间:Follow-up week 12 (FU12)
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Defined as HCV-RNA negativity by a sensitive assay
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Follow-up week 12 (FU12)
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Proportions of Subjects With Adverse Events (AEs) and Serious Adverse Events (SAEs)
大体时间:Baseline (BL) to Follow-up week 12 (FU12)
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Baseline (BL) to Follow-up week 12 (FU12)
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合作者和调查者
调查人员
- 首席研究员:Markus Peck-Radosavljevic, MD、Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna
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 (实际的)
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
- HIVCOBOC-RGT
- 2012-005591-33 (EudraCT编号)
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