A Clinical Trial of 16 Weeks of Duration to Evaluate Retreatment With Elbasvir/Grazoprevir Plus Sofosbuvir and Ribavirin in Patients With Chronic Hepatitis C Genotypes 1,4 Who Have Failed to Treat With a Regime Based on an Inhibitor of the NS5A (C-RESCUE)
2018年6月7日 更新者:Fundacion SEIMC-GESIDA
A Phase III, Open Label, Multicentric Clinical Trial of a Single Arm of 16 Weeks of Duration to Evaluate Retreatment With Elbasvir/Grazoprevir Plus Sofosbuvir and Ribavirin in Patients With Chronic Hepatitis C Genotype 1,4 Who Have Failed to Treat With a Regime Based on an Inhibitor of the NS5A
This is a phase 4 clinical trial to treat patients who have failed to treat with regimen based on an inhibitor of the NS5A
研究概览
详细说明
The duration of the treatment will be 16 weeks and then will be a security perid with 2 visits (Week 12 post treatment and week 24 post treatment) The study in an open label study with a single arm .
研究类型
介入性
阶段
- 第四阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
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Madrid、西班牙、28031
- Hospital Infanta Leonor
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Madrid、西班牙、28007
- Hospital Univ. Gregorio Marañon
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Madrid、西班牙、28041
- Hospita 12 de octubre
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Madrid、西班牙、28046
- Hospital Univ. La Paz
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Madri
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Madrid、Madri、西班牙、28046
- Hospital Univ. La Paz
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Adults with chronic HCV genotype 1, 4 infection with or without HIV infection aged 18 years or above
- HCV RNA plasma concentration of at least 1000 IU / mL
- Subjects previously treated with NS5A-based regimens for at least 8 weeks.
- Patients with HCV relapse after receiving a complete treatment with NS5A-based AAD regimen for at least 8 weeks and becoming undetectable at the end of treatment. Relapse is defined as a confirmed HCV RNA detectable upon completion of therapy of A5 based on NS5A against HCV.
- Subjects with compensated hepatic cirrhosis (Child A) could be included.
For patients with HIV coinfection:
- Be infected with HIV-1, documented by any rapid HIV test with the corresponding license and confirmed by a Western blot or second antibody test using a method other than the initial rapid HIV and / or I / CIA method or by HIV-1 p24 antigen or viral load of HIV-1 RNA plasma.
- Be on stable HIV antiretroviral therapy (ART) for at least 4 weeks prior to entry into the study using a dual ITN backbone of tenofovir or abacavir and emtricitabine or lamivudine PLUS raltegravir or dolutegravir or rilpivirine (with CD4 + T cell count> 100 cells / mm 3 and undetectable HIV-1 RNA at baseline. Results from prior analysis will be accepted within 24 weeks prior to study entry).
Exclusion Criteria:
- Subjects with hepatitis other than C or steatosis.
- Subjects previously treated less than 8 weeks with regimens based on NS5A.
- Evidence of previous hepatocellular carcinoma although it has criteria of cure
- Subjects with past or current decompensated liver disease; Only decompensated patients who have received a liver transplant and have not decompensated after transplantation will be included.
- Subjects suspected of clinical or genotypic reinfection of HCV.
- Subject with HCV response regrowth while receiving NS5A-based ADA therapy against HCV. Said regrowth is defined as a confirmation of detectable HCV RNA after achieving undetectable HCV RNA during NS5A-based AADs against HCV.
- Recent history of drug or alcohol abuse.
Important comorbidities.
- Pregnant, lactating or non-lactating women Contraceptives, if they are women of childbearing age. Women of childbearing age are defined as those women who have not undergone permanent infertility procedures or who have been amenorrheic for less than 12 months.
- Subjects with a glomerular filtration rate of less than 30 ml / min.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 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:Single arm
16 weeks treatment with elbasvir/grazoprevir plus sofosbuvir and ribavirina
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16 weeks treatment
其他名称:
16 weeks treatment
16 weeks treatment
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研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
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The rate of patients achieved SVR12
大体时间:Week 12 post treatment
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Week 12 post treatment
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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The proportion of subjects infected with HCV genotype 1a with reference VARs NS5A / NS3 who achieved RVS12.
大体时间:Week 12 post treatment
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To analyze the impact of VARs NS5A/NS3 on RVS12
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Week 12 post treatment
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The proportion of subjects infected with HCV genotype 1b with reference VARs NS5A / NS3 who achieved RVS12.
大体时间:Week 12 post treatment
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Analyze the impact of VARs NS5A/NS3 on RVS12
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Week 12 post treatment
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The proportion of subjects infected with HCV genotype 4 with reference VARs NS5A /NS3 who achieved RVS12.
大体时间:Week 12 post treatment
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Analyze the impact of VARs NS5A/NS3 on RVS12
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Week 12 post treatment
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The proportion of subjects infected with HCV genotypes 1.4 with reference VARs NS5A /NS3 who achieved RVS24.
大体时间:Week 24 post treatment
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Analyze the impact of VARs NS5A/NS3 on RVS24
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Week 24 post treatment
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The occurrence of Viral resistance variants (VARs) to NS5A or elbasvir, to NS3 or grazoprevir and to NS5B or SOF in patients who did not reach SVR12 after 16 weeks of re-treatment
大体时间:Week 16
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the occurrence of resistance in patients who did not reach SVR12 after 16 weeks of re-treatment
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Week 16
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The occurrence of resistance variants (VARs) viral to NS5A or elbasvir, to NS3 or grazoprevir, and to NS5B or SOF in HIV patients included
大体时间:Week 12 post treatment
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The impact of VARs NS5A/NS3 on RVS12 The proportion of subjects developing HIV-1 virological failure (HIV RNA> 200 Copies / mL), confirmed in 2 consecutive tests with at least 2 weeks between them. |
Week 12 post treatment
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The proportion of subjects developing HIV-1 virological failure (HIV RNA> 200 Copies / mL), confirmed in 2 consecutive tests with at least 2 weeks between them
大体时间:Week 4, week 8, week 12 and week 16
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the impact of treatment with EL / BRA plus SOFT and ribavirin in HIV-1 subjects
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Week 4, week 8, week 12 and week 16
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The proportion of subjects experiencing adverse events of high laboratory values who report as ECI at any time during the study period.
大体时间:Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with at least one adverse experience
大体时间:Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with an adverse experience related to medication
大体时间:Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with a severe adverse experience
大体时间:Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with a serious adverse experience related to medication
大体时间:Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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The proportion of subjects with an adverse experience leading to disruption
大体时间:Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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Adverse events
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Week 4, week 8, week 12, week 16, week 12 post-treatment and week 24 post-treatment
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (预期的)
2017年7月1日
初级完成 (预期的)
2017年12月1日
研究完成 (预期的)
2018年2月1日
研究注册日期
首次提交
2017年3月16日
首先提交符合 QC 标准的
2017年4月6日
首次发布 (实际的)
2017年4月7日
研究记录更新
最后更新发布 (实际的)
2018年6月8日
上次提交的符合 QC 标准的更新
2018年6月7日
最后验证
2018年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
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Assistance Publique Hopitaux De Marseille未知
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National Institutes of Health Clinical Center (CC)Bristol-Myers Squibb; National Institute of Allergy and Infectious Diseases (NIAID)完全的
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University of California, IrvineUniversity of California, Los Angeles; National Institute on Minority Health and Health Disparities...完全的
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National Taiwan University Hospital未知
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Merck Sharp & Dohme LLC完全的
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University Hospital, ToulouseMSD France完全的
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National Cheng-Kung University HospitalMerck Sharp & Dohme LLC完全的
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Oregon Health and Science University完全的
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University of Maryland, BaltimoreMerck Sharp & Dohme LLC; Cairo University撤销
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University of Illinois at ChicagoMerck Sharp & Dohme LLC完全的
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University of Florence未知丙型肝炎 | 冷球蛋白血症性肾小球肾炎
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Erasmus Medical Center完全的
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Merck Sharp & Dohme LLC完全的
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