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High Dose Ribavirin in the Treatment of Chronic Hepatitis C

10 de novembro de 2011 atualizado por: University of Bern

Prospective, Open-label, Randomised Controlled Trial on Efficacy and Tolerability of PegIFN-alpha 2a + Serum Level-adapted RBV vs. PegIFN-alpha 2a + Weight-based RBV in Treatment-naive Patients With Chronic Hepatitis C Genotype 1

Treatment of patients with chronic hepatitis C infected with genotype 1 hepatitis C virus (HCV) consists of combined peginterferon/ribavirin for 48 weeks. Approximately 50% of patients experience sustained virological response which equals cure. All other patients either do not respond or experience recurrence of HCV virus and chronic hepatitis. Important predictors of successful treatment are sustained dosing of both peginterferon and ribavirin. With regard to the latter, clinical evidence indicates that higher ribavirin doses may in fact even improve treatment outcome. However, high ribavirin doses cause hemolytic anemia which require dose reductions. Recent clinical experience show that erythropoetic growth factors, including erythropoetin, can counteract hemolytic anemia caused by antiviral treatment in chronic hepatitis C patients. Therefore, the current trial aims to test whether higher ribavirin doses adapted to a target plasma concentrations instead of a weight-based dosing result in better healing rates, and whether ribavirin-associated hemolytic anemia can be compensated by concommitant erythropoetin treatment.

Using a randomized, controlled, open-label design, the investigators hypothesize that patients with high ribavirin doses adapted to plasma levels experience better viral clearance than patients treated with standard weight-based ribavirin doses. In addition, the investigators hypothesize that erythropoetin treatment will counteract hemolytic anemia induced by ribavirin thereby allowing maintenance of target plasma concentrations without ribavirin dose reductions.

Visão geral do estudo

Descrição detalhada

Background

Prevalence and incidence of chronic hepatitis C (CHC) are rising worldwide. Complications include chronic liver failure and hepatocellular carcinoma, and chronic hepatitis C is a major indication for liver transplantation. Effective treatment is required to prevent these outcomes.

Current treatment consists of a combination of peginterferon (PegIFN) and ribavirin (RBV) given for 24 or 48 weeks depending on the viral genotype. While genotypes 2 and 3 respond well to 24 weeks of PegIFN/RBV with approximately 80% viral clearance, genotype 1 infected patients only achieve about 40-50% sustained viral response (SVR) with 48 weeks of combination therapy.

RBV is a nucleoside analog with structural similarities to guanosine, which modulates RNA and DNA synthesis. RBV reveals antiviral activity against respiratory syncytial (RS)-virus, influenza virus, Lassa virus uand others. The exact mode of antiviral activity is yet unknown but believed to relate to reducing survival of HCV-infected hepatocytes thereby allowing for elimination of infected cells by interferon-stimulated immune mechanisms.

Generally, RBV is well tolerated. With standard daily doses between 1.000 and 1.200mg, irritability, sleeping abnormalities, cough and pruritus. The most prevalent and typical side effect of RBV is a dose-dependent hemolytical anemia which responds well to dose reduction or interruption of RBV therapy. RBV-associated anemia impairs quality of life and, overall, 25-36% of patients require dose reductions and/or RBV cessation. However, reduction/cessation of RBV is associated with a significant drop of SVR and measures to maintain RBV doses are clearly warranted. Several recent studies have shown that erythropoetin can counteract RBV-induced hemolytic anemia, and improve quality of life.

The relevance of RBV dose with regard to therapeutic response to combination therapy is well-established and currently, RBV is dosed according to weight: patients with CHC genotype 1 are treated with 1.000mg if body weight is <65kg, and receive 1.200mg if >65kg.

Retrospective studies have shown that relapsers and non-responders to antiviral treatment with RBV had lower RBV levels than those who had a SVR. In a retrospective analysis of 4 studies investigating a total of 1105 patients treated with RBV, RBV plasma concentrations measured at 4 weeks of treatment correlated with viral clearance: SVR was 31.8% in those with RBV levels <1,000ng/ml, and increased to 62.5% with RBV concentrations at >4,000ng/ml.

A pilot trial from Sweden investigated whether dosing RBV according to a plasma level of 15mcmol/l (3.7mcg/ml) in 10 patients. Median RBV dose was 2.540mg/day and all patients received erythropoetin.SVR was achieved in 9 of 10 patients.

So far, a randomized, controlled trial comparing weight-based RBV (standard) vs. RBV dosed according to kidney function and plasma levels.

Objective

Comparison of efficacy and tolerability of treatment with PegIFN-alpha 2a + RBV dosed according plasma concentrations vs PegIFN-alpha 2a + weight-based RBV in patients with chronic hepatitis C genotype 1

Methods

Prospective, controlled, open label randomized human trial

Tipo de estudo

Intervencional

Inscrição (Real)

32

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

      • Basel, Suíça, CH-4031
        • Dept of Gastroenterology, University of Basel
      • Bern, Suíça, CH-3010
        • Institute of Clinical Pharmacology and Visceral Research, University of Bern
      • Lausanne, Suíça, CH-1011
        • Division of Gastroenterology, University of Lausanne
      • St. Gallen, Suíça, CH-9007
        • Kantonsspital St.Gallen
      • Zürich, Suíça, Ch-8037
        • Stadtspital Waid, Zürich

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos a 65 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Male and female patients aged 18-65 years
  • Elevated liver enzymes levels
  • Compensated liver disease
  • Available liver histology confirming METAVIR F2 fibrosis
  • Written consent to participation

Exclusion Criteria

  • Age <18, >65
  • Prior ribavirin treatment
  • Intolerance towards ribavirin, PegIFN or erythropoetin
  • Pregnancy or breast feeding
  • Relevant cardiovascular or pulmonary disease
  • Kidney insufficiency (creatinine clearance <50ml/min)
  • Coinfection with HIV or hepatitis B virus
  • Hepatic comorbidities (hemochromatosis, Wilson's disease, autoimmune disorders)
  • Alcohol consumption > 40g/day
  • Psychiatric disorders
  • Malignancy (except for basalioma)
  • Active consumption of illicit drugs
  • Participation in another trial shorter than 3 months prior to inclusion
  • Lack of consent

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: A
PegIFN-alpha 2a + RBV (commenced according to kidney function) adjusted to plasma levels. Treatment with erythropoetin 3x3,000IU/week up to 3x10,000IU/week in case of hemolytic anemia
Ribavirin dose started according to kidney function (usually 1,800mg) and adapted according to plasma level during follow-up
Comparador Ativo: B
PegIFN-alpha 2a + RBV (weight based; 1,000 or 1,200 mg/day)
Ribavirin dose started at 1,000mg (body weight <65kg) or 1,200mg (body weight equal or >65kg)

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Sustained virological response
Prazo: 1 Day
1 Day

Medidas de resultados secundários

Medida de resultado
Prazo
Adverse Events
Prazo: day 1 until 24 weeks after end or treatment
day 1 until 24 weeks after end or treatment
Rapid virological response at 4 weeks of treatment
Prazo: 4 weeks
4 weeks
Early virological response at 12 weeks of treatment
Prazo: 12 weeks
12 weeks

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Investigador principal: Felix Stickel, MD, Institute for Clinical Pharmacology and Visceral Research, University of Bern

Publicações e links úteis

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo

1 de novembro de 2007

Conclusão Primária (Real)

1 de abril de 2011

Conclusão do estudo (Real)

1 de abril de 2011

Datas de inscrição no estudo

Enviado pela primeira vez

17 de julho de 2009

Enviado pela primeira vez que atendeu aos critérios de CQ

21 de julho de 2009

Primeira postagem (Estimativa)

23 de julho de 2009

Atualizações de registro de estudo

Última Atualização Postada (Estimativa)

11 de novembro de 2011

Última atualização enviada que atendeu aos critérios de controle de qualidade

10 de novembro de 2011

Última verificação

1 de novembro de 2011

Mais Informações

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Ensaios clínicos em Hepatite C crônica

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