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Utilization of Hepatitis C Positive Kidneys in Negative Recipients

Primary Purpose

Kidney Transplant, Hepatitis C, HCV

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Sofosbuvir / Velpatasvir Oral Tablet [Epclusa]
Glecaprevir/Pibrentasvir 100 MG-40 MG Oral Tablet [MAVYRET]
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Kidney Transplant

Eligibility Criteria

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

Recipient Inclusion/Exclusion Criteria:

Inclusion Criteria:

  • Adult age >18 years able to provide consent
  • Lack of available living donor
  • Calculated pre-transplant reactive panel (cPRA) of <80%
  • Estimated post-transplant survival (EPTS) index >20% and <80%
  • Negative pre-transplant human immunodeficiency virus (HIV), HCV, and hepatitis B virus (HBV) serology and blood HCV PCR
  • No clinically significant pre-transplant liver disease

Exclusion Criteria:

  • Living donor available
  • Dialysis time >5 years
  • Listing for multi-organ transplantation
  • Active or recent history (<6 months) of alcohol abuse or substance abuse
  • Clinically significant liver disease as determined by principal investigator
  • History of hepatocarcinoma
  • Pregnancy or lactation
  • Refusal to accept blood transfusion
  • HIV infection
  • HCV pcr or antibody positive
  • HBV infection

Donor Inclusion Criteria:

  • Positive HCV PCR at time of donation
  • Kidney donor profile index (KDPI)<85%

Sites / Locations

  • Brenda Cuson

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention group

Arm Description

kidney transplant recipients who receive kidney allograft from hepatitis C viremic donors followed by treatment with direct acting antiviral therapies.

Outcomes

Primary Outcome Measures

Proportion of Patients With Undetectable Hepatitis C Virus (HCV) Polymerase Chain Reaction (PCR) at 12 Weeks After Completion of HCV Treatment
Proportion of patients with undetectable hepatitis C virus (HCV) polymerase chain reaction (PCR) at 12 weeks after completion of HCV treatment was to test the efficacy of the treatment.
Elevation in Liver Enzyme >5 Times the Upper Limits, Development of Acute Cholestatic Hepatitis , or Intolerance to Direct Acting Antiviral Therapies
Elevation in liver enzyme >5 times the upper limits, development of acute cholestatic hepatitis , or intolerance to Direct acting antiviral therapies was to test the safety of utilizing HepC positive kidneys for transplant.

Secondary Outcome Measures

Estimated Glomerular Filtration Rate (eGFR) at 6 and 12 Months Post-transplant
Estimated glomerular filtration rate (eGFR) at 6 and 12 months post-transplant was to test the safety of utilizing of HepC positive kidneys.
Patient's Survival at 6 and 12 Months
Patient's survival at 6 and 12 months measuring safety of utilizing of HepC positive kidneys.
Graft Survival at 6 and 12 Months
Graft survival at 6 and 12 months measuring safety of utilizing HepC positive kidneys.

Full Information

First Posted
January 9, 2019
Last Updated
August 30, 2023
Sponsor
Ohio State University
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1. Study Identification

Unique Protocol Identification Number
NCT03801707
Brief Title
Utilization of Hepatitis C Positive Kidneys in Negative Recipients
Official Title
An Open Label, Proof of Concept Study to Evaluate the Feasibility and Safety of Kidney Transplant From HCV Positive Donors Into HCV Negative Recipient
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
March 22, 2019 (Actual)
Primary Completion Date
April 28, 2021 (Actual)
Study Completion Date
April 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To evaluate the safety and feasibility of transplanting kidneys from Hepatitis C virus (HCV) infected donors into recipients without HCV infection
Detailed Description
This will be an open label, prospective, interventional, proof of concept study to evaluate the feasibility and safety of kidney transplant from HCV positive donors into HCV negative recipients using treatment with pan-genotypic direct acting antiviral therapies (DAAS) for treatment of post-transplant HCV transmission

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Transplant, Hepatitis C, HCV

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
kidney transplant recipients who receive kidney allograft from hepatitis C viremic donors followed by treatment with direct acting antiviral therapies.
Intervention Type
Drug
Intervention Name(s)
Sofosbuvir / Velpatasvir Oral Tablet [Epclusa]
Other Intervention Name(s)
Epclusa
Intervention Description
fixed dose combination medication once a day for 12 weeks for the treatment of hepatitis C
Intervention Type
Drug
Intervention Name(s)
Glecaprevir/Pibrentasvir 100 MG-40 MG Oral Tablet [MAVYRET]
Other Intervention Name(s)
Mavyret
Intervention Description
Three tablets once a day for 12 weeks for treatment of hepatitis C
Primary Outcome Measure Information:
Title
Proportion of Patients With Undetectable Hepatitis C Virus (HCV) Polymerase Chain Reaction (PCR) at 12 Weeks After Completion of HCV Treatment
Description
Proportion of patients with undetectable hepatitis C virus (HCV) polymerase chain reaction (PCR) at 12 weeks after completion of HCV treatment was to test the efficacy of the treatment.
Time Frame
12 weeks
Title
Elevation in Liver Enzyme >5 Times the Upper Limits, Development of Acute Cholestatic Hepatitis , or Intolerance to Direct Acting Antiviral Therapies
Description
Elevation in liver enzyme >5 times the upper limits, development of acute cholestatic hepatitis , or intolerance to Direct acting antiviral therapies was to test the safety of utilizing HepC positive kidneys for transplant.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Estimated Glomerular Filtration Rate (eGFR) at 6 and 12 Months Post-transplant
Description
Estimated glomerular filtration rate (eGFR) at 6 and 12 months post-transplant was to test the safety of utilizing of HepC positive kidneys.
Time Frame
6 and 12 months
Title
Patient's Survival at 6 and 12 Months
Description
Patient's survival at 6 and 12 months measuring safety of utilizing of HepC positive kidneys.
Time Frame
6 and 12 months
Title
Graft Survival at 6 and 12 Months
Description
Graft survival at 6 and 12 months measuring safety of utilizing HepC positive kidneys.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Recipient Inclusion/Exclusion Criteria: Inclusion Criteria: Adult age >18 years able to provide consent Lack of available living donor Calculated pre-transplant reactive panel (cPRA) of <80% Estimated post-transplant survival (EPTS) index >20% and <80% Negative pre-transplant human immunodeficiency virus (HIV), hepatitis C virus (HCV), and hepatitis B virus (HBV) serology and blood HCV polymerase chain reaction (PCR) No clinically significant pre-transplant liver disease Exclusion Criteria: Living donor available Dialysis time >5 years Listing for multi-organ transplantation Active or recent history (<6 months) of alcohol abuse or substance abuse Clinically significant liver disease as determined by principal investigator History of hepatocarcinoma Pregnancy or lactation Refusal to accept blood transfusion HIV infection HCV pcr or antibody positive HBV infection Donor Inclusion Criteria: Positive HCV PCR at time of donation Kidney donor profile index (KDPI)<85%
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Reem Daloul, MD
Organizational Affiliation
Ohio State University School of Biomedical Science: The Ohio State University College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brenda Cuson
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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Results Reference
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Links:
URL
https://www.usrds.org/annual-data-report/current-adr/
Description
USRDS Annual Data Report 2017

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Utilization of Hepatitis C Positive Kidneys in Negative Recipients

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