Viral kinetic models of HCV clearance in hemophiliacs treated with telaprevir
特拉匹韦治疗血友病患者 HCV 清除的病毒动力学模型
基本信息
- 批准号:8302090
- 负责人:
- 金额:$ 37.22万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2012
- 资助国家:美国
- 起止时间:2012-05-25 至 2014-04-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAntiviral AgentsBloodClinicalClinical TreatmentClinical TrialsClinical Trials DesignDataDevelopmentDiseaseEvaluationEvolutionFundingGoalsHIVHealthHemophilia AHemorrhageHepatitis CHepatitis C virusImmune responseImmunocompetentInfectionInheritedInterferon Alfa-2aInterferonsInterventionKineticsLaboratory StudyLeadLiverLiver diseasesModalityModelingMorbidity - disease rateMulticenter Hemophilia Cohort StudyMulticenter TrialsOutcomeOutcome AssessmentPatientsPegylated Interferon AlfaPersonal CommunicationPharmaceutical PreparationsPhasePhase III Clinical TrialsPilot ProjectsPrevalenceProtease InhibitorRandomized Controlled TrialsRegimenRelative (related person)RibavirinRiskSafetySeveritiesStagingTechniquesTestingTimeUnited States National Institutes of HealthViralabstractingattributable mortalitybaseblood productcohortexperienceimprovedinnovationmathematical modelmortalitynamed groupresistance mutationresponsesmall moleculestandard of caretherapy durationtreatment responseviral resistance
项目摘要
DESCRIPTION (provided by applicant):
Infection with the hepatitis C virus is an important contributor to morbidity and mortality among those with hemophilia and other inherited bleeding disorders in whom such infections are common. Current treatment modalities using pegylated-interferon alfa and ribavirin are suboptimal in terms of response. New small molecules targeted to inhibition of HCV replication offer promise in terms of improved response rates, and shorter durations of therapy, but their use has not been assessed in special populations, including those with hemophilia and related disorders. Furthermore, the optimal regimen which provides high efficacy with low levels of development of viral resistance to the experimental agent has not been established. This pilot study will examine the efficacy and safety of two strategies utilizing telaprevir in combination with pegylated- interferon alfa/ribavirin. Using powerful mathematical modeling techniques we will explore first and second phase kinetic responses to treatment in patients with inherited bleeding disorders who are either treatment na¿ve or treatment experienced (interferon-based HCV treatment). Specifically our aims are 1: Development and implementation of a pilot clinical trial designed to assess dynamic kinetic response parameters and safety of telaprevir combined with standard of care therapy in subjects with inherited bleeding disorders, and 2: To evaluate prevalence and rate of emergence of class-specific resistance mutations to protease inhibitors and to identify early predictors of mutational selection. This study will inform development of a large, multicenter trial that would follow completion of the pilot phase proposed herein.
PUBLIC HEALTH RELEVANCE:
Hepatitis C infection is an important cause of severe disease in patients with hemophilia. Treatment of hepatitis C with interferon-based therapies is the mainstay of current treatment but is inadequate due to relatively poor response rates in terms of viral clearance. Telaprevir is a new direct acting antiviral agent that appears to improve treatment response when combined with interferon and ribavirin, and has not been tested in patients with inherited bleeding disorders.
(End of Abstract)
描述(由申请人提供):
丙型肝炎病毒感染是血友病和其他遗传性出血性疾病患者发病率和死亡率的一个重要因素,这些感染在这些患者中很常见。目前使用聚乙二醇干扰素α和利巴韦林的治疗方式在反应方面是次优的。靶向抑制HCV复制的新小分子在改善应答率和缩短治疗持续时间方面提供了希望,但尚未评估其在特殊人群(包括血友病和相关疾病患者)中的使用。此外,还没有建立提供高疗效和低水平的病毒对实验药物的耐药性发展的最佳方案。该初步研究将检查特拉匹韦与聚乙二醇干扰素α/利巴韦林联合使用的两种策略的疗效和安全性。使用强大的数学建模技术,我们将探讨第一和第二阶段的动力学反应,治疗遗传性出血性疾病的患者谁是初治或治疗经验丰富(干扰素为基础的HCV治疗)。具体来说,我们的目标是1:开发和实施一项试点临床试验,旨在评估特拉匹韦联合标准治疗在遗传性出血性疾病受试者中的动态动力学反应参数和安全性,2:评估蛋白酶抑制剂类特异性耐药突变的发生率和发生率,并确定突变选择的早期预测因子。本研究将为在完成本文拟定的试验阶段后开展一项大型多中心试验提供信息。
公共卫生相关性:
丙型肝炎感染是血友病患者重症的重要原因。用基于干扰素的疗法治疗丙型肝炎是目前治疗的主要方法,但由于在病毒清除方面的应答率相对较低而不足。特拉匹韦是一种新的直接作用的抗病毒药物,当与干扰素和利巴韦林联合使用时,似乎可以改善治疗反应,但尚未在遗传性出血性疾病患者中进行过测试。
(End摘要)
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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KENNETH E SHERMAN其他文献
KENNETH E SHERMAN的其他文献
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{{ truncateString('KENNETH E SHERMAN', 18)}}的其他基金
Biomarkers of Replication and Injury in HBV/HIV
HBV/HIV 复制和损伤的生物标志物
- 批准号:
10449351 - 财政年份:2021
- 资助金额:
$ 37.22万 - 项目类别:
Biomarkers of Replication and Injury in HBV/HIV
HBV/HIV 复制和损伤的生物标志物
- 批准号:
10326569 - 财政年份:2021
- 资助金额:
$ 37.22万 - 项目类别:
Viral kinetic models of HCV clearance in hemophiliacs treated with telaprevir
特拉匹韦治疗血友病患者 HCV 清除的病毒动力学模型
- 批准号:
8472526 - 财政年份:2012
- 资助金额:
$ 37.22万 - 项目类别:
Antiretroviral Therapy and the Hepatitis C Virus
抗逆转录病毒治疗和丙型肝炎病毒
- 批准号:
7062999 - 财政年份:2006
- 资助金额:
$ 37.22万 - 项目类别:
HIV Antiretroviral Therapy and Hepatic Injury
HIV 抗逆转录病毒治疗和肝损伤
- 批准号:
9139029 - 财政年份:2006
- 资助金额:
$ 37.22万 - 项目类别:
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