NCT06774144
Rezafungin Prophylaxis in Liver Transplant
Enrolling by Invitation
PHASE3Ages 18+InterventionalPreventionFernanda P Silveira, MD, MSInvestigator-initiated
~385 participants
Updated 2025-10-20 on ClinicalTrials.gov
What's tested:RezafunginStandard of care antifungal prophylaxis
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of proven and probable IFIs
Measured over 90 days post-transplant
+1 more outcome measured
Conditions
Where it's being run
1 sites across 1 statesPennsylvania1
Study leadership
- Fernanda Silveira · PRINCIPAL_INVESTIGATOR · University of Pittsburgh
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Liver transplant recipient
18 years of age or older
≥1 risk factor(s) for IFI: living donor transplant, retransplantation, complicated operations (based on duration of transplant and number of blood products required in the peri-transplant period), choledochojejunostomy anastomosis, or peri-operative Candida colonization, recent Candida infection, renal replacement therapy post-transplant, and reoperation within the first 90 days of transplant.
Exclusion
Participants who are perceived not to survive past 7 days after transplant
Participants who elect not to participate in the prospective trial
Participants who had active candidiasis at the time of transplant
Participants with a history of allergy to an echinocandin
Participants who are pregnant.
What this trial measures
- Incidence of proven and probable IFIs90 days post-transplant
Incidence of proven and probable IFIs within 90 days post-transplant
- Incidence of proven and probable breakthrough IFIWhile receiving rezafungin, voriconazole, or fluconazole
Incidence of breakthrough IFI while on specific antifungal prophylaxis