Lung Transplant Recipient

3

Review clinical trials related to Lung Transplant Recipient. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

BRIDGE - Blocking Receptor of IL-1β for Donor Graft Edema Reduction

This study will determine if primary graft dysfunction (which causes low blood oxygen levels and fluid or inflammation in the lungs) after lung transplant can be prevented through the use of the study drug (IL-1 receptor antagonist, Anakinra). In this study, lung transplant participants who are randomized to the treatment group will have the study drug injected into the solution that their donor lungs are kept in prior to transplant.

Participants needed: 20
Trial details
Phase: Early Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Northwestern UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Age 18 years or older. [+3]

Previous or current use of IL-1R antagonist drug. [+1]

Status: Recruiting

Combination Letermovir and Standard of Care Antiviral for Enhanced Antiviral Response in Cytomegalovirus Infection in Lung Transplant Recipients

The primary objective of the CLEAR-CMV trial is to evaluate the efficacy of letermovir therapy plus standard of care (SOC) antiviral compared to SOC plus placebo in achieving clearance of CMV viremia by week 3 in lung transplant recipients with active CMV infection.

Participants needed: 40
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University Health Network, TorontoUpdated: Feb 17, 2026Locations: 1
Eligibility criteria

Recipient of a lung transplant. [+1]

Renal failure with Creatinine clearance <15 mL/min or requiring dialysis [+7]

Status: Recruiting

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

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

Participants needed: 20
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: University Health Network, TorontoUpdated: Nov 17, 2025Locations: 1
Eligibility criteria

HBV SAg positive and/or HBV NAT+ donor

HIV positive [+14]