A Single-arm Evaluation of the Effect of HCV Treatment on Cardiovascular Disease Risk (HEART-C)
A Single-arm Evaluation of the Effect of Elbasvir/Grazoprevir on Cardiometabolic Parameters in Patients With Hepatitis C Infection and Underlying Metabolic Disease
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Tipo di studio
Tipo di studio
Fase
Fase
- Fase 4
Contatti e Sedi
Luoghi di studio
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-
California
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Los Angeles, California, Stati Uniti, 90025
- UCLA CARE Center
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-
Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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:
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
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Altro
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
|
Sperimentale: All participants
Intervention: Elbasvir/grazoprevir
|
Daily fixed-dose combination (FDC) elbasvir (EBR) (50 mg)/grazoprevir (GZR) (100 mg) for 12 weeks
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Change in reactive hyperemia index (RHI) by peripheral arterial tonometry (PAT)
Lasso di tempo: Baseline to 12 weeks after end of EBR/GZR treatment.
|
Baseline to 12 weeks after end of EBR/GZR treatment.
|
Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Change in insulin resistance by HOMA-IR
Lasso di tempo: Baseline to 12 weeks after end of treatment
|
Baseline to 12 weeks after end of treatment
|
|
Change in reactive hyperemia index (RHI) by PAT
Lasso di tempo: Baseline to week 4 on treatment
|
Baseline to week 4 on treatment
|
|
Change in reactive hyperemia index (RHI) by PAT
Lasso di tempo: Baseline to 52 weeks after end of treatment
|
Baseline to 52 weeks after end of treatment
|
|
Change in insulin resistance by HOMA-IR
Lasso di tempo: Baseline to week 4 on treatment
|
Baseline to week 4 on treatment
|
|
Change in insulin resistance by HOMA-IR
Lasso di tempo: Baseline to 52 weeks after end of treatment
|
Baseline to 52 weeks after end of treatment
|
|
Change in hemoglobin A1c
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
|
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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
Lasso di tempo: Baseline, week 4, post-treatment weeks 12 and 52
|
Baseline, week 4, post-treatment weeks 12 and 52
|
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Cross-sectional fibrosis score in kPa by transient elastography (TE) for correlation with RHI and soluble biomarkers
Lasso di tempo: 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
Lasso di tempo: Baseline and 12 and 52 weeks after end of treatment
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Baseline and 12 and 52 weeks after end of treatment
|
|
Change in fibrosis score by transient elastography
Lasso di tempo: Baseline to 52 weeks after end of treatment
|
Baseline to 52 weeks after end of treatment
|
|
Change in hepatic steatosis score by CAP
Lasso di tempo: Baseline to 52 weeks after end of treatment
|
Baseline to 52 weeks after end of treatment
|
Collaboratori e investigatori
Sponsor
Sponsor
Collaboratori
Collaboratori
Investigatori
Investigatori
- Investigatore principale: Kara W Chew, M.D., M.S., University of California, Los Angeles
Studiare le date dei record
Studia le date principali
Inizio studio (Anticipato)
Inizio studio
Completamento primario (Anticipato)
Completamento primario
Completamento dello studio (Anticipato)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie dell'apparato digerente
- Infezioni da virus a RNA
- Malattie virali
- Infezioni
- Infezioni a trasmissione ematica
- Malattie trasmissibili
- Malattie del fegato
- Flaviviridae Infezioni
- Epatite, virale, umana
- Infezioni da enterovirus
- Infezioni da Picornaviridae
- Malattia cardiovascolare
- Epatite
- Epatite A
- Epatite C
- Malattie metaboliche
- Agenti antinfettivi
- Agenti antivirali
- Grazoprevir
- Combinazione di farmaci Elbasvir-grazoprevir
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- 18-000650
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Informazioni su farmaci e dispositivi, documenti di studio
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