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Recruiting Phase 4 NCT07189377

NCT07189377 Combined Light, ExVivo, and Antivirals for Recipients of Lungs From HBV Donors

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Clinical Trial Summary
NCT ID NCT07189377
Status Recruiting
Phase Phase 4
Sponsor University Health Network, Toronto
Condition Hepatitis B Virus (HBV)
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2025-09-24
Primary Completion 2027-08

Trial Parameters

Condition Hepatitis B Virus (HBV)
Sponsor University Health Network, Toronto
Study Type INTERVENTIONAL
Phase Phase 4
Enrollment 20
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-09-24
Completion 2027-08
Interventions
EntecavirHBIGEVLP UV Light Treatment

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Brief Summary

The aim of the study is to show that transplantation of lungs from Hepatitis B-infected donors is safe when using EVLP with UV light inactivation plus antivirals

Eligibility Criteria

Donor Inclusion Criteria * Donor lung suitable for transplantation * HBV SAg positive and/or HBV NAT+ donor Donor Exclusion Criteria * HIV positive * HTLV 1/2 positive; * Any medical issues in the donor that would normally clinically exclude the donor (e.g. history of cancer, evidence of organ dysfunction, etc). Recipient inclusion Criteria: * Recipients eligible and listed for lung transplant * HBV NAT negative * Provides written informed consent * Has received at least 3 prior doses of Hepatitis B vaccine or anti-HBs\>=10 IU/mL * Patients with other co-morbid conditions (such as diabetes, autoimmune disease, renal dysfunction) will remain eligible provided they are otherwise medically suitable for transplantation. The exception to this will be patients with significant liver disease as outlined below. Recipient exclusion Criteria: * Chronic liver disease with \> stage 2 fibrosis * Participating in another interventional clinical trial * Recipient listed for combined transplant (e.g.,

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