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Grazoprevir/Elbasvir for Genotype 1b Chronic Hepatitis C After Liver or Kidney Transplantation

Primary Purpose

Chronic Hepatitis c, Liver Transplant Infection, Kidney Transplant Infection

Status
Terminated
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
grazoprevir 100 mg/ elbasvir 50 mg, Zepatier®
Sponsored by
Taichung Veterans General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Hepatitis c

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. At least 20 years of age
  2. Chronically infected with genotypes 1b HCV
  3. Underwent liver and/ or kidney transplantation
  4. Without clinical or pathologic evidence of moderate or severe rejection

Exclusion Criteria:

  1. HCV genotype other than 1b
  2. Liver decompensation (Child-Pugh score > 6)
  3. Co-infected with human immunodeficiency virus: Positive HIV1/2 or hepatitis B virus : Positive HBsAg and detected HBV DNA
  4. Prior exposure to an NS5A inhibitor
  5. Any active malignancies
  6. Hemoglobin level less than 10 g/dl
  7. Platelet level of 75,000/mm3 or less
  8. Alanine aminotransferase, aspartate aminotransferase, or alkaline phosphatase level 10 times or more the upper limit of normal
  9. Total bilirubin level greater than 3 times or more the upper limit of normal
  10. Albumin less than 3 g/dL
  11. Using medication that is not considered safe to co-administer with , such as cyclosporine
  12. Pregnant or breast-feeding women
  13. Known allergy to grazoprevir or elbasvir

(Unregistered liver or kidney transplant in other countries is illegal in Taiwan)

Sites / Locations

  • Taichung Veterans General Hospital
  • China Medical University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Zepatier therapy

Arm Description

grazoprevir 100 mg/ elbasvir 50 mg (Zepatier®, MSD) once daily for 12 weeks

Outcomes

Primary Outcome Measures

Sustained virologic response (SVR)
The HCV viral load (IU/mL) in blood at post-treatment week 12 (SVR12)

Secondary Outcome Measures

Adverse effects (AEs)
Any AEs during the treatment period
Used immunosuppressant blood levels
The immunosuppressant concentration (ng/mL) in blood during the treatment period

Full Information

First Posted
October 26, 2018
Last Updated
March 14, 2021
Sponsor
Taichung Veterans General Hospital
Collaborators
Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT03723824
Brief Title
Grazoprevir/Elbasvir for Genotype 1b Chronic Hepatitis C After Liver or Kidney Transplantation
Official Title
An Open-label, Cohort Study of Grazoprevir/Elbasvir Combination Therapy for Patients With Genotype 1b Chronic Hepatitis C After Liver or Kidney Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Terminated
Why Stopped
COV-19 pandemic
Study Start Date
February 14, 2019 (Actual)
Primary Completion Date
November 30, 2020 (Actual)
Study Completion Date
March 13, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Taichung Veterans General Hospital
Collaborators
Merck Sharp & Dohme LLC

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Grazoprevir/elbasvir combination therapy is highly effective in the treatment of genotype 1b chronic hepatitis C, and the drug-drug interaction with central immunosuppressant, such as tacrolimus, should be manageable. The aim of this study is to assess the efficacy and tolerability of grazoprevir/elbasvir combination therapy in treating genotype 1b chronic hepatitis C after liver or kidney transplantation.
Detailed Description
Grazoprevir/elbasvir combination therapy (grazoprevir 100 mg/ elbasvir 50 mg, Zepatier®, MSD) has been recommended as the 1st-line treatment for genotype 1b chronic hepatitis C by the updated international guidelines, and the rates of sustained virologic response (SVR) can be higher than 95% in either treatment-naïve or peginterferon-experienced patients with genotype 1b chronic hepatitis C. Moreover, even among patients with liver cirrhosis, the efficacy of grazoprevir/elbasvir combination therapy remains very high. In addition, drug-related adverse effects (AEs) were quite low in previous studies, and less than 1% of cirrhotic patients discontinued this therapy during treatment period (4). Grazoprevir/elbasvir combination therapy is an effective and safe treatment for chronic hepatitis C. Chronic hepatitis C is one of the most common indications for liver transplantation. Patients underwent liver or kidney transplantation always suffer from recurrent chronic hepatitis C. Recurrent chronic hepatitis C can result in liver cirrhosis, liver decompensation, and death. Chronic hepatitis C is also associated with a higher incidence of chronic rejection, graft failure and mortality after kidney transplantation. Treating hepatitis C virus (HCV) infection after liver or kidney transplantation was a big challenge before the development of new direct-acting antiviral (DAA). Not only a low SVR rate but also a high rate of severe adverse effects results in the hesitation of peginterferon-ribavirin combination therapy. Although some new DAAs can be used in organ transplantation, the cost remains quite high. More new DAA choices for patients underwent organ transplantation are needed. The clinical data of grazoprevir/elbasvir combination therapy on the treatment for patients with chronic hepatitis C after liver or kidney transplantation remain lacking. With high virologic response rates and low adverse effects in the management for chronic hepatitis C, grazoprevir/elbasvir combination therapy could be a good option for patients underwent liver or kidney transplantation. No drug-drug interaction (DDI) was noted between grazoprevir/elbasvir combination therapy and steroid, and the DDI with the most commonly-used immunosuppressant, tacrolimus, was also not significant, The drug levels of immunosuppressants can be carefully monitored and adjusted during treatment period. The aim of this study is to assess the efficacy and tolerability of grazoprevir/elbasvir combination therapy in treating genotype 1b chronic hepatitis C after liver or kidney transplantation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hepatitis c, Liver Transplant Infection, Kidney Transplant Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Model Description
grazoprevir 100 mg/ elbasvir 50 mg, Zepatier®, 1# qd for 12 weeks
Masking
None (Open Label)
Allocation
N/A
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Zepatier therapy
Arm Type
Experimental
Arm Description
grazoprevir 100 mg/ elbasvir 50 mg (Zepatier®, MSD) once daily for 12 weeks
Intervention Type
Drug
Intervention Name(s)
grazoprevir 100 mg/ elbasvir 50 mg, Zepatier®
Other Intervention Name(s)
Zepatier
Intervention Description
grazoprevir 100 mg/ elbasvir 50 mg (Zepatier®, MSD) once daily for 12 weeks
Primary Outcome Measure Information:
Title
Sustained virologic response (SVR)
Description
The HCV viral load (IU/mL) in blood at post-treatment week 12 (SVR12)
Time Frame
At post-treatment week 12
Secondary Outcome Measure Information:
Title
Adverse effects (AEs)
Description
Any AEs during the treatment period
Time Frame
During the treatment period (the 1st, 2nd, 4th, 6th, 8th, 10th, 12th weeks)
Title
Used immunosuppressant blood levels
Description
The immunosuppressant concentration (ng/mL) in blood during the treatment period
Time Frame
During the treatment period (the 1st, 2nd, 4th, 6th, 8th, 10th, 12th weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least 20 years of age Chronically infected with genotypes 1b HCV Underwent liver and/ or kidney transplantation Without clinical or pathologic evidence of moderate or severe rejection Exclusion Criteria: HCV genotype other than 1b Liver decompensation (Child-Pugh score > 6) Co-infected with human immunodeficiency virus: Positive HIV1/2 or hepatitis B virus : Positive HBsAg and detected HBV DNA Prior exposure to an NS5A inhibitor Any active malignancies Hemoglobin level less than 10 g/dl Platelet level of 75,000/mm3 or less Alanine aminotransferase, aspartate aminotransferase, or alkaline phosphatase level 10 times or more the upper limit of normal Total bilirubin level greater than 3 times or more the upper limit of normal Albumin less than 3 g/dL Using medication that is not considered safe to co-administer with , such as cyclosporine Pregnant or breast-feeding women Known allergy to grazoprevir or elbasvir (Unregistered liver or kidney transplant in other countries is illegal in Taiwan)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Teng-Yu Lee, MD
Organizational Affiliation
Taichung Veterans General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Taichung Veterans General Hospital
City
Taichung
ZIP/Postal Code
40705
Country
Taiwan
Facility Name
China Medical University Hospital
City
Taichung
Country
Taiwan

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25909356
Citation
Zeuzem S, Ghalib R, Reddy KR, Pockros PJ, Ben Ari Z, Zhao Y, Brown DD, Wan S, DiNubile MJ, Nguyen BY, Robertson MN, Wahl J, Barr E, Butterton JR. Grazoprevir-Elbasvir Combination Therapy for Treatment-Naive Cirrhotic and Noncirrhotic Patients With Chronic Hepatitis C Virus Genotype 1, 4, or 6 Infection: A Randomized Trial. Ann Intern Med. 2015 Jul 7;163(1):1-13. doi: 10.7326/M15-0785.
Results Reference
result
PubMed Identifier
27720838
Citation
Kwo P, Gane EJ, Peng CY, Pearlman B, Vierling JM, Serfaty L, Buti M, Shafran S, Stryszak P, Lin L, Gress J, Black S, Dutko FJ, Robertson M, Wahl J, Lupinacci L, Barr E, Haber B. Effectiveness of Elbasvir and Grazoprevir Combination, With or Without Ribavirin, for Treatment-Experienced Patients With Chronic Hepatitis C Infection. Gastroenterology. 2017 Jan;152(1):164-175.e4. doi: 10.1053/j.gastro.2016.09.045. Epub 2016 Oct 5.
Results Reference
result
PubMed Identifier
28193518
Citation
Jacobson IM, Lawitz E, Kwo PY, Hezode C, Peng CY, Howe AYM, Hwang P, Wahl J, Robertson M, Barr E, Haber BA. Safety and Efficacy of Elbasvir/Grazoprevir in Patients With Hepatitis C Virus Infection and Compensated Cirrhosis: An Integrated Analysis. Gastroenterology. 2017 May;152(6):1372-1382.e2. doi: 10.1053/j.gastro.2017.01.050. Epub 2017 Feb 11.
Results Reference
result
PubMed Identifier
34902265
Citation
Lai PC, Chen CH, Jeng LB, Yu TM, Tsai SF, Wu MJ, Cheng SB, Yang SS, Lee TY. Grazoprevir/Elbasvir Treatment in Liver or Kidney Transplant Recipients with Genotype 1b Hepatitis C Virus Infection. Antimicrob Agents Chemother. 2022 Feb 15;66(2):e0200321. doi: 10.1128/AAC.02003-21. Epub 2021 Dec 13.
Results Reference
derived

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Grazoprevir/Elbasvir for Genotype 1b Chronic Hepatitis C After Liver or Kidney Transplantation

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