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
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Fase
Fase
- Fase 4
Kontakter og lokationer
Studiesteder
-
-
California
-
Los Angeles, California, Forenede Stater, 90025
- UCLA CARE Center
-
-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
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
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Eksperimentel: All participants
Intervention: Elbasvir/grazoprevir
|
Daily fixed-dose combination (FDC) elbasvir (EBR) (50 mg)/grazoprevir (GZR) (100 mg) for 12 weeks
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change in reactive hyperemia index (RHI) by peripheral arterial tonometry (PAT)
Tidsramme: Baseline to 12 weeks after end of EBR/GZR treatment.
|
Baseline to 12 weeks after end of EBR/GZR treatment.
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change in insulin resistance by HOMA-IR
Tidsramme: Baseline to 12 weeks after end of treatment
|
Baseline to 12 weeks after end of treatment
|
|
Change in reactive hyperemia index (RHI) by PAT
Tidsramme: Baseline to week 4 on treatment
|
Baseline to week 4 on treatment
|
|
Change in reactive hyperemia index (RHI) by PAT
Tidsramme: Baseline to 52 weeks after end of treatment
|
Baseline to 52 weeks after end of treatment
|
|
Change in insulin resistance by HOMA-IR
Tidsramme: Baseline to week 4 on treatment
|
Baseline to week 4 on treatment
|
|
Change in insulin resistance by HOMA-IR
Tidsramme: Baseline to 52 weeks after end of treatment
|
Baseline to 52 weeks after end of treatment
|
|
Change in hemoglobin A1c
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: Baseline to 52 weeks after end of treatment
|
Baseline to 52 weeks after end of treatment
|
|
Change in hepatic steatosis score by CAP
Tidsramme: Baseline to 52 weeks after end of treatment
|
Baseline to 52 weeks after end of treatment
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Samarbejdspartnere
Samarbejdspartnere
Efterforskere
Efterforskere
- Ledende efterforsker: Kara W Chew, M.D., M.S., University of California, Los Angeles
Datoer for undersøgelser
Studer store datoer
Studiestart (Forventet)
Studiestart
Primær færdiggørelse (Forventet)
Primær færdiggørelse
Studieafslutning (Forventet)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Sygdomme i fordøjelsessystemet
- RNA-virusinfektioner
- Virussygdomme
- Infektioner
- Blodbårne infektioner
- Overførbare sygdomme
- Leversygdomme
- Flaviviridae infektioner
- Hepatitis, viral, menneskelig
- Enterovirus infektioner
- Picornaviridae infektioner
- Hjerte-kar-sygdomme
- Hepatitis
- Hepatitis A
- Hepatitis C
- Metaboliske sygdomme
- Anti-infektionsmidler
- Antivirale midler
- Grazoprevir
- Elbasvir-grazoprevir lægemiddelkombination
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- 18-000650
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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