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Completed

NCT Number: NCT02858180

Hepatitis C Virus(HCV) Heart and Lung Study

This is a multicenter study in Hepatitis C Virus (HCV) infected adult patients who also have advanced cardiac disease or advanced lung disease.

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Key information

About this study

This is a multicenter study in HCV infected adult patients who also have either advanced cardiac disease, or advanced lung disease. Advanced cardiac disease is defined as a marked limitation of physical activity, or discomfort upon physical activity. The patients in the advanced cardiac disease group must also have been hospitalized for heart failure within the last 12 months.

Advanced lung disease is defined as patients who have been diagnosed with chronic obstructive pulmonary disease (COPD) or interstitial lung disease (ILD). Patients in the COPD group must have abnormalities in their forced expiratory volume (FEV) test, which measures the amount of air exhaled. They may or may not need supplemental oxygen. Patients in the ILD group must have been diagnosed with ILD and require supplement oxygen at all times.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Chronic HCV Infection of Genotype 1, 4, 5, or 6
  • HCV RNA > 103 IU/mL at screening
  • 18 years of age or older
  • Diagnosis of chronic HCV infection, defined as positive HCV antibody or HCV RNA more than 6 months prior to screening OR an assessment of fibrosis F2 or greater prior to screening.

Subjects in the advanced heart failure cohort must meet all HCV criteria, and all of the following criteria:

  • New York Heart Association (NYHA) Class III or IV functional classification
  • NYHA Class III: Subjects with cardiac disease resulting in marked limitation of physical activity. They are comfortable at rest. Less than ordinary physical activity causes fatigue, palpitation, dyspnea, or anginal pain.
  • NYHA Class IV: Patient with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms of cardiac insufficiency or of the anginal syndrome may be present even at rest. If any physical activity is undertaken, discomfort is increased.
  • ejection fraction ≤ 30%
  • hospitalized for heart failure in last 12 months

Subjects in the advanced lung disease cohort must have been diagnosed with chronic obstructive pulmonary disease (COPD) or interstitial lung disease (ILD) must meet all HCV criteria, and meet the following criteria for COPD or ILD:

  • ILD criteria: diagnosis of interstitial lung disease with chronic supplemental oxygen requirement at rest and/or with exertion.
  • COPD criteria (one of the following):
  • Forced expiratory volume (FEV1)< 30% predicted
  • OR any FEV1 with chronic supplemental oxygen requirement at rest and/or with exertion
  • OR any FEV1 with chronic hypercapnia (baseline partial pressure of arterial carbon dioxide [PaCO2] > 45)

Exclusion criteria

  • Chronic HCV Infection with Genotype 2 or 3
  • Treatment with any of the following agents
  • Amiodarone. Subjects previously treated with amiodarone must have stopped the amiodarone at least 60 days prior to day 1 of SOF/LDV FDC
  • Carbamazepine, phenytoin, phenobarbital, oxcarbazepine
  • Rifabutin, rifampin or rifapentine
  • HIV regimens containing tenofovir or tipranavir/ritonavir
  • St. John's wort
  • Rosuvastatin
  • Have any serious or active medical or psychiatric illness which, in the opinion of the investigator, would interfere with subject treatment, assessment, or compliance
  • History of hepatic encephalopathy or variceal hemorrhage
  • Hepatitis B surface antigen positive
  • Abnormal hematological and biochemical parameters, including:
  • Hemoglobin (Hb) < 8 g/dL
  • Platelets ≤ 50,000/mm3
  • alanine aminotransferase (ALT), aspartase aminotransferase (AST), or alkaline phosphatase ≥ 10 times upper limit of normal(ULN)
  • Total bilirubin > 3 mg/dl
  • Severe renal impairment creatinine clearance (CrCl), i.e. < 30 mL/min.
  • History of major organ transplantation with an existing functional graft.
  • History of clinically-significant drug allergy to nucleoside/nucleotide analogs.
  • Pregnant women or women planning to become pregnant
  • Women who are breastfeeding
  • Active or recent history (≤ 1 year) of drug or alcohol abuse

Treatment and study plan

Sofosbuvir/ledipasvir fixed dose combination(SOF/LDV FDC)

Drug

1 pill once daily of SOF/LDV FDC

Other names: Harvoni

Primary outcomes

  1. Number of Subjects Who Completed 24 Weeks of Therapy

    Time frame: 24 weeks

    The primary safety endpoint is the number of subjects who complete a full course of therapy.

Secondary outcomes

  1. Number of Subjects With Sustained Virologic Response (SVR) 12

    Time frame: 12 weeks after completing treatment

    The secondary outcome of efficacy will be determined by the number of subjects with hepatitis c virus ribonucleic acid (HCV RNA) below a measurable laboratory limit, 12 weeks after completing therapy.

  2. Number of Subjects With Sustained Virologic Response (SVR) 4

    Time frame: 4 weeks after completing treatment

    The secondary outcome of efficacy will be determined by the number of subjects with hepatitis c virus ribonucleic acid (HCV RNA) below a measurable laboratory limit, 4 weeks after completing treatment.

Other outcomes

  1. Discontinuation for Adverse Events and Serious Adverse Events

    Time frame: 12 weeks after completing treatment

    Assessment for discontinuation due to adverse events and serious adverse events, as addressed by adverse events and laboratory tests. Final study visit is 12 weeks after treatment.

Sponsors and collaborators

Lead sponsor

Duke University

Other

Collaborators

  • Gilead Sciences

Registry information

Official study title

A Multicenter, Open-label Study of Harvoni ® (Sofosbuvir Ledipasvir Fixed Dose Combination) in Subjects Infected With Chronic Hepatitis C and Advanced Heart Failure or Lung Disease

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Aug 8, 2016
Registry last updated
Apr 21, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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