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

3 augustus 2018 bijgewerkt door: 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.

Studie Overzicht

Toestand

Ingetrokken

Conditie

Interventie / Behandeling

Studietype

Ingrijpend

Fase

  • Fase 4

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • California
      • Los Angeles, California, Verenigde Staten, 90025
        • UCLA CARE Center

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Ander
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: All participants
Intervention: Elbasvir/grazoprevir
Daily fixed-dose combination (FDC) elbasvir (EBR) (50 mg)/grazoprevir (GZR) (100 mg) for 12 weeks
Andere namen:
  • Zepatier, serial number 86336186

Wat meet het onderzoek?

Primaire uitkomstmaten

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

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Change in insulin resistance by HOMA-IR
Tijdsspanne: Baseline to 12 weeks after end of treatment
Baseline to 12 weeks after end of treatment
Change in reactive hyperemia index (RHI) by PAT
Tijdsspanne: Baseline to week 4 on treatment
Baseline to week 4 on treatment
Change in reactive hyperemia index (RHI) by PAT
Tijdsspanne: Baseline to 52 weeks after end of treatment
Baseline to 52 weeks after end of treatment
Change in insulin resistance by HOMA-IR
Tijdsspanne: Baseline to week 4 on treatment
Baseline to week 4 on treatment
Change in insulin resistance by HOMA-IR
Tijdsspanne: Baseline to 52 weeks after end of treatment
Baseline to 52 weeks after end of treatment
Change in hemoglobin A1c
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Baseline to 52 weeks after end of treatment
Baseline to 52 weeks after end of treatment
Change in hepatic steatosis score by CAP
Tijdsspanne: Baseline to 52 weeks after end of treatment
Baseline to 52 weeks after end of treatment

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

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

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Verwacht)

1 augustus 2018

Primaire voltooiing (Verwacht)

1 juni 2019

Studie voltooiing (Verwacht)

1 april 2020

Studieregistratiedata

Eerst ingediend

29 juni 2018

Eerst ingediend dat voldeed aan de QC-criteria

29 juni 2018

Eerst geplaatst (Werkelijk)

12 juli 2018

Updates van studierecords

Laatste update geplaatst (Werkelijk)

7 augustus 2018

Laatste update ingediend die voldeed aan QC-criteria

3 augustus 2018

Laatst geverifieerd

1 augustus 2018

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Ja

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

product vervaardigd in en geëxporteerd uit de V.S.

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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