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Trial record 62 of 82 for:    GRAZOPREVIR ANHYDROUS AND ELBASVIR

EBR/GZR for HCV-1b Patients Receiving Hemodialysis

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT03420300
Recruitment Status : Active, not recruiting
First Posted : February 5, 2018
Last Update Posted : May 22, 2019
Information provided by (Responsible Party):
National Taiwan University Hospital

Brief Summary:
Hepatitis C virus (HCV) infection is common in patients receiving hemodialysis. The uptake of antiviral therapy for these patients is limited in the era of interferon (IFN) plus ribavirin (RBV), probably because the sustained virologic response (SVR) rates are low and the risk of treatment-related adverse events (AEs) are high. In the era of IFN-free direct acting antiviral agents (DAAs), several studies have indicated high rates of SVR and excellent safety profiles to treat patients with severe renal impairment. With regard to elbasvir/grazoprevir (EBR/GZR) treatment, a phase 3 study (C-SURFER) study has shown 99% of SVR in HCV-1 patients with chronic kidney disease (CKD) stage 4 or 5. Furthermore, most patients tolerated the treatment well. Although the data confirmed the excellent safety and efficacy in HCV-1 patients with severe renal impairment, data regarding the safety and efficacy for Asian HCV-1b patients receiving hemodialysis is lacking. Therefore, we aim to evaluated the safety and efficacy of EBR/GZR for 12 weeks in treatment-naive and treatment-experienced HCV-1b patients receiving hemodialysis.

Condition or disease Intervention/treatment Phase
Hepatitis C Drug: EBR/GZR Phase 4

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 40 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Elbasvir/Grazoprevir for Treatment-naive and Treatment-experienced Patients With Hepatitis C Virus Genotype 1b Receiving Hemodialysis
Actual Study Start Date : June 5, 2018
Estimated Primary Completion Date : November 25, 2019
Estimated Study Completion Date : February 20, 2020

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: EBR/GZR
Elbasvir/grazoiprevir (EBR/GZR 50mg/100mg fixed dose combination [FDC]): 1 table per os per day for 12 weeks
Elbasvir/grazoiprevir (EBR/GZR 50mg/100mg fixed dose combination [FDC]): 1 table per os per day for 12 weeks
Other Name: Zepatier

Primary Outcome Measures :
  1. Sustained virologic response (SVR12) [ Time Frame: 24 weeks ]
    Undetectable serum HCV RNA 12 weeks off therapy (treatment period 12 weeks)

Secondary Outcome Measures :
  1. Treatment-emergent adverse event (AE)-related withdrawal rate [ Time Frame: 12 weeks ]
    Treatment-emergent adverse event (AE)-related withdrawal rate

  2. Sustained virologic response (SVR24) [ Time Frame: 36 weeks ]
    Undetectable serum HCV RNA 24 weeks off therapy (treatment period 12 weeks)

  3. Rapid virologic response (RVR) [ Time Frame: 4 weeks ]
    Undetectable serum HCV RNA at week 4 of treatment

  4. End-of-treatment virological response (EOTVR) [ Time Frame: 12 weeks ]
    Undetectable serum HCV RNA at week 12 of treatment

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   20 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • 20 yeas or more
  • Male or female
  • Body mass index (BMI) 18.5-35.0 kg/m2
  • Chronic HCV infection, defined as patients who meet as least one of the two following criteria:

    1. Anti-HCV antibody (Abbott HCV EIA 2.0, Abbott Laboratories, Abbott Park, Illinois, USA) or HCV RNA > 1,000 IU/mL for at least 6 months before screening
    2. Positive HCV RNA > 1,0000 IU/mL (Cobas TaqMan HCV Test v2.0, Roche Diagnostics GmbH, Mannheim, Germany, low limit of quantification (LLOQ): 25 IU/mL) at the time of screening with a liver biopsy consistent with chronic HCV infection
  • HCV genotype 1 (HCV GT-1b) infection (Abbott RealTime HCV genotype II, Abbott Molecular Inc. Illinois, USA)
  • Treatment-naïve or treatment-experienced (including patients who relapsed, who had virological breakthrough, or who were null-responsive to IFN-based therapies)
  • HCV RNA > 10,000 IU/mL at screening
  • Estimated glomerular filtration (eGFR) rate < 15 mL/min/1.73m2 as assessed by modified of diet in renal disease (MDRD) equation, and receiving regular hemodialysis

Exclusion Criteria:

  • HCV infection other than HCV GT-1b
  • HBV or HIV coinfection
  • Presence of decompensated cirrhosis (Child-Pugh class B or C)
  • Any primary cause of liver disease other than chronic HCV infection, including but not limited to the following

    1. Hemochromatosis
    2. Alfa-1 antitrypsin deficiency
    3. Wilson's disease
    4. Autoimmune hepatitis
    5. Alcoholic liver disease
    6. Drug-induced hepatitis
    7. Screening laboratory analyses showing any of the following results

      • Hemoglobin (Hb) level < 10 g/dL
      • Absolute neutrophil count (ANC) < 1,500 cells/μL
      • Platelet count < 70,000 cells/mm3
      • International normalized ratio (INR) > 2.0
      • Albumin (Alb)< 3.0 g/dL
      • Bilirubin (Bil) > 2.0 mg/dL
      • Alanine aminotransferase (ALT) > 10X upper limit of normal (ULN)
      • Aspartate aminotransferase (AST) > 10X upper limit of normal (ULN)
      • Serum alfa-fetoprotein (AFP) > 100 ng/mL
  • Presence of hepatocellular carcinoma (HCC) on imaging studies such as computed tomography (CT) scan or magnetic resonance imaging (MRI)
  • History of malignancy (except cutaneous melanoma) within 5 years at the screening
  • Organ transplantation other than cornea and hair (prior renal transplantation with graft failure not included)
  • Prior exposure to investigational agents for HCV (direct acting antiviral agents, host-targeting agents, or therapeutic vaccines)
  • Pregnancy
  • Unwilling to have contraception during the study period
  • Unwilling to provide informed consent

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03420300

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National Taiwan University Hospital, Yun-Lin Branch
Douliu, Taiwan
China Medical University Hospital
Taichung, Taiwan
Taichung Veterans General Hospital
Taichung, Taiwan
Far Eastern Memorial Hospital
Taipei county, Taiwan
National Taiwan University Hospital
Taipei, Taiwan
Taipei Medical University
Taipei, Taiwan
Sponsors and Collaborators
National Taiwan University Hospital
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Study Director: Chen-Hua Liu, MD, PhD National Taiwan University Hospital

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Responsible Party: National Taiwan University Hospital Identifier: NCT03420300    
Other Study ID Numbers: 201709053MIPC
First Posted: February 5, 2018    Key Record Dates
Last Update Posted: May 22, 2019
Last Verified: May 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: Confidential of the individual participant data

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by National Taiwan University Hospital:
Hepatitis C virus
Direct acting antiviral agent
Additional relevant MeSH terms:
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Hepatitis A
Hepatitis C
Liver Diseases
Digestive System Diseases
Hepatitis, Viral, Human
Virus Diseases
Enterovirus Infections
Picornaviridae Infections
RNA Virus Infections
Flaviviridae Infections