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Lung Transplant HCV, Pilot Study

Primary Purpose

Lung Transplant Infection, Hepatitis C

Status
Active
Phase
Early Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Sofosbuvir-velpatasvir (400 mg/100 mg)
Ex Vivo Lung Perfusion (EVLP)
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lung Transplant Infection focused on measuring Lung, Transplant, Hepatitis C, DAAs, Epclusa

Eligibility Criteria

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

Inclusion Criteria:

  • Recipients listed for single or bilateral lung transplant
  • HCV Nucleic Acid Amplification Testing (NAT) negative
  • Ability to provide written informed consent

Exclusion Criteria:

  • Participation in another interventional clinical trial

Sites / Locations

  • University Health Network Toronto General Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

HCV+ lung transplant to HCV- recipients

Arm Description

HCV+ donor lungs will be treated with Normothermic Ex Vivo Lung Perfusion (EVLP) in order to reduce viral load and minimize risk of HCV transmission. Patients who become viremic defined as at least two consecutive positive samples will receive sofosbuvir/velpatasvir 400 mg/100 mg (Epclusa) for 12 weeks.

Outcomes

Primary Outcome Measures

Safety of transplantation from HCV positive donors to HCV negative recipients
Safety of transplantation using HCV positive donors reflected by 6 month survival and being free of HCV by PCR (either due to lack of transmission or as a result of treatment).

Secondary Outcome Measures

Incidence of HCV transmission
Incidence of donor to recipient HCV transmission.
Correlation between viral loads and recipient infection
Correlation between donor viremia, EVLP perfusate virus load (PCR), lung tissue virus load at the end of EVLP (PCR) and recipient infection
Time to viremia development
Interval of time from transplantation to development of viremia
HCV cure rates
HCV cure rates after treatment of infected patients

Full Information

First Posted
April 6, 2017
Last Updated
November 10, 2022
Sponsor
University Health Network, Toronto
Collaborators
Gilead Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT03112044
Brief Title
Lung Transplant HCV, Pilot Study
Official Title
Lung Transplantation Using Hepatitis C Positive Donors to Hepatitis C Negative Recipients: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
September 19, 2017 (Actual)
Primary Completion Date
January 2, 2020 (Actual)
Study Completion Date
April 17, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
Gilead Sciences

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
In this study HCV negative recipients will be transplanted with HCV positive lungs. Investigators will attempt to decrease infectivity rates by performing Normothermic Ex vivo Lung Perfusion (EVLP), which is an approved method of donor lung preservation, assessment and treatment, and could be an excellent platform to reduce/eliminate hepatitis C virus. Patients will be treated by the standard approved direct-acting antivirals (DAAs) if infection occurs. It is planned to enrolled 20 patients from the Lung transplant wait list in this study. Patients will be followed for 6 months. This will be a single center pilot study.
Detailed Description
The success of lung transplantation (LTx) is significantly hindered by the lack of sufficient number of available donors. Many potential donor lungs cannot be utilized in clinical transplantation because donors have chronic viral infections such as hepatitis C (HCV) infection. This study will test the possibility of safely transplanting lungs from HCV positive donors. Donor lungs will be subjected to Normothermic Ex vivo Lung Perfusion (EVLP) for 6 hours for organ assessment and reduction of viral load prior to transplantation. After transplantation, recipients will be carefully monitored for HCV infection and if infection occurs, they will be promptly treated with highly effective antiviral therapy using newly approved DAAs. The aim of the study is to show that transplantation of lungs from HCV positive donors is safe in the era of DAAs. The hypothesis is that the rate of HCV transmission to recipients will be lower than previously described due to EVLP pre-treatment and any HCV transmission that does occur will be readily treatable and curable. If successful, the knowledge from this study can have a large impact to patients with end stage organ diseases by providing a large novel source of donors for lung and potentially other organ transplantations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Transplant Infection, Hepatitis C
Keywords
Lung, Transplant, Hepatitis C, DAAs, Epclusa

7. Study Design

Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Model Description
Investigators aim to transplant 20 HCV- recipients with end-stage lung disease from transplant wait-list using lungs from HCV+ donors. Donor lungs will be selected based on usual donor selection criteria evaluating blood gas analysis, chest imaging, bronchoscopy findings, and assessment in the operating room. Once lungs meet criteria for transplantation, they will be retrieved in standard fashion, transported to Toronto General Hospital in cold static preservation, placed on EVLP for 6 hours, and transplanted to consented recipients.
Masking
None (Open Label)
Allocation
N/A
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HCV+ lung transplant to HCV- recipients
Arm Type
Experimental
Arm Description
HCV+ donor lungs will be treated with Normothermic Ex Vivo Lung Perfusion (EVLP) in order to reduce viral load and minimize risk of HCV transmission. Patients who become viremic defined as at least two consecutive positive samples will receive sofosbuvir/velpatasvir 400 mg/100 mg (Epclusa) for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Sofosbuvir-velpatasvir (400 mg/100 mg)
Other Intervention Name(s)
Epclusa
Intervention Description
Patients will have standard monitoring with HCV RNA and liver panel assessment at 2 week intervals until HCV is undetectable and then at the end of treatment and 3 and 6 months following its completion. Post-operative transplant care and immunosuppression will be carried on as usual transplant practice at Toronto General Hospital.
Intervention Type
Device
Intervention Name(s)
Ex Vivo Lung Perfusion (EVLP)
Other Intervention Name(s)
Normothermic EVLP
Intervention Description
Normothermic EVLP is a method of donor lung preservation, assessment, treatment, and repair of injured organs. This method allows donor lungs to be treated for at least 12h under protective physiological conditions.
Primary Outcome Measure Information:
Title
Safety of transplantation from HCV positive donors to HCV negative recipients
Description
Safety of transplantation using HCV positive donors reflected by 6 month survival and being free of HCV by PCR (either due to lack of transmission or as a result of treatment).
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Incidence of HCV transmission
Description
Incidence of donor to recipient HCV transmission.
Time Frame
6 months
Title
Correlation between viral loads and recipient infection
Description
Correlation between donor viremia, EVLP perfusate virus load (PCR), lung tissue virus load at the end of EVLP (PCR) and recipient infection
Time Frame
6 months
Title
Time to viremia development
Description
Interval of time from transplantation to development of viremia
Time Frame
6 months
Title
HCV cure rates
Description
HCV cure rates after treatment of infected patients
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Recipients listed for single or bilateral lung transplant HCV Nucleic Acid Amplification Testing (NAT) negative Ability to provide written informed consent Exclusion Criteria: Participation in another interventional clinical trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcelo Cypel, MD MSc FRCSC
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network Toronto General Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2N2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31606437
Citation
Cypel M, Feld JJ, Galasso M, Pinto Ribeiro RV, Marks N, Kuczynski M, Kumar D, Bahinskaya I, Bagnato VS, Kurachi C, Slutsky AS, Yeung JC, Donahoe L, de Perrot M, Yasufuku K, Pierre A, Binnie M, Chaparro C, Martinu T, Chen M, Tikkanen J, Chow CW, Sidhu A, Waddell TK, Keshavjee S, Singer LG, Humar A. Prevention of viral transmission during lung transplantation with hepatitis C-viraemic donors: an open-label, single-centre, pilot trial. Lancet Respir Med. 2020 Feb;8(2):192-201. doi: 10.1016/S2213-2600(19)30268-1. Epub 2019 Oct 9.
Results Reference
derived

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Lung Transplant HCV, Pilot Study

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