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Search / Trial NCT06774144

Rezafungin Prophylaxis in Liver Transplant

Launched by FERNANDA P SILVEIRA, MD, MS · Jan 8, 2025

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Rezafungin Liver Transplant Prophylaxis

ClinConnect Summary

This clinical trial is looking at a new medication called rezafungin to see if it can help prevent serious fungal infections in people who have recently received a liver transplant. Fungal infections can be a significant risk for these patients, and the study will compare the outcomes of those who receive rezafungin to those who had a liver transplant in the last two years without this medication.

To be eligible for the trial, participants must be at least 18 years old and have received a liver transplant. They should have one or more factors that increase their risk for fungal infections, such as having a living donor transplant or undergoing complicated surgery. However, individuals who are expected not to survive beyond seven days after the transplant or who have a history of allergy to similar medications cannot participate. This trial is not yet recruiting, but once it starts, participants will have the opportunity to contribute to important research that could improve care for future liver transplant patients.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 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 Criteria:
  • 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.

About Fernanda P Silveira, Md, Ms

Dr. Fernanda P. Silveira, MD, MS, is a distinguished clinical trial sponsor with a robust background in medical research and clinical practice. With a dual expertise in medicine and a Master of Science degree, Dr. Silveira is committed to advancing healthcare through innovative clinical trials. Her focus encompasses a range of therapeutic areas, where she aims to enhance patient outcomes and contribute to the development of effective treatments. Known for her rigorous adherence to ethical standards and regulatory compliance, Dr. Silveira fosters collaboration among multidisciplinary teams to drive research excellence and translate findings into meaningful clinical applications.

Locations

Pittsburgh, Pennsylvania, United States

Patients applied

0 patients applied

Trial Officials

Fernanda Silveira

Principal Investigator

University of Pittsburgh

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported