PF-Atlas › Clinical Trials › NCT05285878
Fingolimod for the Abrogation of Interstitial Fibrosis and Tubular Atrophy Following Kidney Transplantation
Fingolimod · Phase 2
Registry ID
NCT05285878
Phase
Phase 2
Status
Enrolling by invitation
Drug / intervention
Fingolimod
Sponsor
The Methodist Hospital Research Institute
Start
2022-07-28
Enrollment
20
Locations
1
About this trial
This is a randomized, double-blind, placebo-controlled trial in de novo kidney transplant patients to determine if the addition of fingolimod (brand name Gilenya®, candidate name- FTY720) on the background of standard immunosuppression will prevent expansion of the interstitial compartment of the transplanted kidney. Interstitial expansion is the precursor of interstitial fibrosis and graft loss. The study will test the hypothesis that abgrogating the fibrogenic effects of both the RhoA and mTOR pathways with fingolimod will reduce structural damage in transplanted kidneys and possible subsequent transplant failure.
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Medical disclaimer. This page summarizes public trial data for NCT05285878 for information only. It is not medical advice, an endorsement, or an offer to enroll. Confirm details on ClinicalTrials.gov and with a qualified physician.