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A Single-arm Evaluation of the Effect of HCV Treatment on Cardiovascular Disease Risk (HEART-C)

3 de agosto de 2018 atualizado por: Kara Chew, University of California, Los Angeles

A Single-arm Evaluation of the Effect of Elbasvir/Grazoprevir on Cardiometabolic Parameters in Patients With Hepatitis C Infection and Underlying Metabolic Disease

This study will assess the effect of treatment for hepatitis C virus (HCV) on cardiovascular disease risk. The study will enroll men and women who are infected with HCV and have underlying metabolic disease. All participants will receive a 12-week course of an HCV treatment (elbasvir/grazoprevir). Cardiovascular disease risk will be evaluated at baseline, week 4 on treatment, 12 weeks post-treatment, and 52 weeks post-treatment through noninvasive measurements of endothelial function, insulin resistance, liver fibrosis and steatosis, and circulating blood biomarkers.

Visão geral do estudo

Status

Retirado

Condições

Intervenção / Tratamento

Tipo de estudo

Intervencional

Estágio

  • Fase 4

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

    • California
      • Los Angeles, California, Estados Unidos, 90025
        • UCLA CARE Center

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 e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Men and women ≥ 18 years of age.
  • Presence of HCV infection for at least 12 weeks
  • Serum or plasma HCV RNA > lower limit of quantification or detection at any time before or at the time of screening, and the absence of intervening HCV treatment
  • Absence of HIV infection
  • HCV treatment-naïve OR HCV treatment-experienced with PEG-IFN/RBV only (no prior HCV DAA exposure)
  • Genotype 1 or 4 HCV infection. If HCV genotype 1a infection is present, absence of genotype 1a NS5A resistance associated substitutions (RASs) at amino acid positions 28, 30, 31, and 93 must be documented at screening
  • Evidence of metabolic disease defined as:

    1. Insulin resistance or impaired glucose tolerance by one of the following:

      • HOMA-IR ≥2.5 at screening
      • Hemoglobin A1c 5.7-6.4% at screening
      • Diabetes mellitus with hemoglobin A1c <7% at screening and never on more than one oral hypoglycemic agent, as well as never requiring insulin

      OR

    2. Metabolic Syndrome, defined as at least 3 of the following:

      • Waist circumference ≥102 cm for men and ≥ 88 cm for women
      • Serum triglyceride level ≥150 mg/dL or on a triglyceride lowering agent
      • Serum high-density lipoprotein (HDL) cholesterol <40 mg/dL in men and <50 mg/dL in women or drug treatment for low HDL cholesterol
      • Blood pressure ≥130/85 mmHg or drug treatment for elevated blood pressure
      • Fasting blood glucose ≥100 mg/dL
  • Ability and willingness of subject to provide written informed consent

Exclusion Criteria:

  • History of decompensated liver disease (Child Pugh Class B or C)
  • Albumin below 3 g/dL
  • Platelet count below 75,000
  • HBsAg positivity.
  • Pregnancy or breastfeeding
  • Inability to conform to the following drug interruptions for PAT testing, whether due to safety (determined by the investigator) or willingness: No caffeine or recreational or prescription stimulant use for 24 hours prior; no nicotine for 4 hours prior; no vigorous exercise for 12 hours prior; stopping of beta blockers, short-acting calcium channel blockers (CCBs), nitrates, angiotensin-converting enzyme inhibitors (ACE-Is), angiotensin-receptor blockers (ARBs), and renin-inhibitors for 24 hours prior; and stopping of long acting CCBs 48 hours prior to testing.
  • Use of anticoagulant or antiplatelet agents (other than aspirin ≤ 325 mg orally daily) within 1 week prior to study entry or anticipated need for these agents for >7 days during the study follow-up period.
  • Use of contraindicated concomitant medications, including OATP1B1/3 inhibitors and strong CYP3A inducers
  • Serious illness including acute liver-related disease and malignancy requiring systemic treatment or hospitalization within 12 weeks prior to study entry.
  • History of major organ transplantation with an existing functional graft and on immunosuppressive therapy.
  • History of known vascular disorder or autoimmune processes including Crohn's disease, ulcerative colitis, severe psoriasis, rheumatoid arthritis, and cryoglobulinemia that may affect vascular studies.
  • Decompensated congestive heart failure or acute cardiovascular event (such as stroke, myocardial infarction, arrhythmia, acute peripheral arterial insufficiency) within 6 months prior to study entry
  • Use of immune-based therapies or systemic corticosteroids which may affect vascular studies or inflammatory/endothelial biomarkers within 12 weeks prior to study entry
  • Advanced renal insufficiency as defined by glomerular filtration rate (GFR) < 30 mL/min/1.73 m2 or treatment by dialysis
  • Anticipated inability to comply with research study visits as determined by the investigator
  • Poor venous access not allowing screening laboratory collection
  • Having any condition that the investigator considers a contraindication to study participation

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: Outro
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: All participants
Intervention: Elbasvir/grazoprevir
Daily fixed-dose combination (FDC) elbasvir (EBR) (50 mg)/grazoprevir (GZR) (100 mg) for 12 weeks
Outros nomes:
  • Zepatier, serial number 86336186

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Change in reactive hyperemia index (RHI) by peripheral arterial tonometry (PAT)
Prazo: Baseline to 12 weeks after end of EBR/GZR treatment.
Baseline to 12 weeks after end of EBR/GZR treatment.

Medidas de resultados secundários

Medida de resultado
Prazo
Change in insulin resistance by HOMA-IR
Prazo: Baseline to 12 weeks after end of treatment
Baseline to 12 weeks after end of treatment
Change in reactive hyperemia index (RHI) by PAT
Prazo: Baseline to week 4 on treatment
Baseline to week 4 on treatment
Change in reactive hyperemia index (RHI) by PAT
Prazo: Baseline to 52 weeks after end of treatment
Baseline to 52 weeks after end of treatment
Change in insulin resistance by HOMA-IR
Prazo: Baseline to week 4 on treatment
Baseline to week 4 on treatment
Change in insulin resistance by HOMA-IR
Prazo: Baseline to 52 weeks after end of treatment
Baseline to 52 weeks after end of treatment
Change in hemoglobin A1c
Prazo: Baseline to week 4, baseline to 12 weeks after end of treatment, and baseline to 52 weeks after end of treatment
Baseline to week 4, baseline to 12 weeks after end of treatment, and baseline to 52 weeks after end of treatment
Change in total and LDL cholesterol levels
Prazo: Baseline to week 4, baseline to 12 weeks after end of treatment, and baseline to 52 weeks after end of treatment
Baseline to week 4, baseline to 12 weeks after end of treatment, and baseline to 52 weeks after end of treatment
Change in levels of each soluble biomarker (sCD163, sCD14, sICAM-1, PAI-1, sE-selectin, oxidized LDL, Lp-PLA2, and lipoprotein particle quantification)
Prazo: Baseline to week 4, baseline to 12 weeks after end of treatment, and baseline to 52 weeks after end of treatment
Baseline to week 4, baseline to 12 weeks after end of treatment, and baseline to 52 weeks after end of treatment
Cross-sectional levels of each soluble biomarker (sCD163, sCD14, sICAM-1, PAI-1, sE-selectin, oxidized LDL, Lp-PLA2, and lipoprotein particle quantification) at each time point for correlation with RHI
Prazo: Baseline, week 4, post-treatment weeks 12 and 52
Baseline, week 4, post-treatment weeks 12 and 52
Cross-sectional fibrosis score in kPa by transient elastography (TE) for correlation with RHI and soluble biomarkers
Prazo: Baseline and 12 and 52 weeks after end of treatment
Baseline and 12 and 52 weeks after end of treatment
Cross-sectional steatosis score in dB/m by CAP for correlation with RHI and soluble biomarkers at the same time points
Prazo: Baseline and 12 and 52 weeks after end of treatment
Baseline and 12 and 52 weeks after end of treatment
Change in fibrosis score by transient elastography
Prazo: Baseline to 52 weeks after end of treatment
Baseline to 52 weeks after end of treatment
Change in hepatic steatosis score by CAP
Prazo: Baseline to 52 weeks after end of treatment
Baseline to 52 weeks after end of treatment

Colaboradores e Investigadores

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

Colaboradores

Investigadores

  • Investigador principal: Kara W Chew, M.D., M.S., University of California, Los Angeles

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 (Antecipado)

1 de agosto de 2018

Conclusão Primária (Antecipado)

1 de junho de 2019

Conclusão do estudo (Antecipado)

1 de abril de 2020

Datas de inscrição no estudo

Enviado pela primeira vez

29 de junho de 2018

Enviado pela primeira vez que atendeu aos critérios de CQ

29 de junho de 2018

Primeira postagem (Real)

12 de julho de 2018

Atualizações de registro de estudo

Última Atualização Postada (Real)

7 de agosto de 2018

Última atualização enviada que atendeu aos critérios de controle de qualidade

3 de agosto de 2018

Última verificação

1 de agosto de 2018

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

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 .

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