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A Randomized Pilot Study of Treatment for Subclinical Antibody-Mediated Rejection in Kidney Transplant Recipients
This is a pilot study to determine if extended release Envarsus at an optimal level is just as effective as more invasive standard therapies for subclinical (mild) AMR (antibody mediated rejection) in kidney transplant patients. Subjects will be randomized to either conversion to Envarsus XR (extended release); or, to a standard of care regimen of plasma exchange/IVIG (intravenous immunoglobulin)/rituximab treatments.
There is currently minimal data to guide treatment of mild graft damage in kidney transplant patients. Some of the current therapies used often come with dangerous complications (infections, malignancies, etc.). This is a pilot study to determine if extended release Envarsus at an optimal level is just as effective as more invasive standard therapies for subclinical (mild) AMR (antibody mediated rejection) in kidney transplant patients. The subjects will be randomized to either conversion from their current tacrolimus regimen to Envarsus XR (a once a day, extended release version of tacrolimus); or, to a regimen of 5 plasma exchanges/IVIG (intravenous immunoglobulin) treatments and one treatment with rituximab. Subjects who are within their first year of transplant will visit their doctor monthly for regular tests and checks and then will have a kidney biopsy at 6 months. Subjects who had their transplant over a year prior will see the doctor for tests and checks at 1, 3 and 5 months and then will have a biopsy of the kidney at month 6.
Age
18 - 79 years
Sex
ALL
Healthy Volunteers
No
University of Colorado Anschutz Medical Campus
Aurora, Colorado, United States
Start Date
January 17, 2018
Primary Completion Date
October 16, 2019
Completion Date
October 16, 2019
Last Updated
October 27, 2020
4
ACTUAL participants
Tacrolimus Extended Release Oral Tablet [Envarsus]
DRUG
Plasma Exchange and IVIG (Intravenous Immunoglobulin )
OTHER
Lead Sponsor
University of Colorado, Denver
Collaborators
NCT07006532
NCT04736381
NCT04702022
Data Source & Attribution
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