CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 176 enrolled
Drug / intervention
Prograf +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02866682
NCT02866682Phase 4Completed

Prospective Study Comparing Brand and Generic Immunosuppression on Transplant Outcomes, Adherence, & Immune Response

University of California, Los Angeles·interventional·Posted Aug 15, 2016·Updated Apr 28, 2023

In Brief

A Phase 4 clinical trial evaluating Prograf and Tacrolimus for Renal Transplant Rejection. Completed, enrolled 176 participants across 1 site.

Detailed Summary

As the patents for brand-name immunosuppressive medications expire, there is increasing interest in using generic immunosuppressive drugs. However, despite pharmacokinetic studies showing bioequivalence, questions remain regarding the clinical impact of use of generic immunosuppression. The most important immunosuppressive agent in the modern transplant era is arguably tacrolimus, a calcineurin-inhibitor with a narrow therapeutic index. This study seeks to answer the question regarding the clinical impact of generic tacrolimus use as measured primarily by acute rejection, loss of graft function, and patient death through a randomized trial of 2 phases: Brand tacrolimus only, and Generic A tacrolimus only. Given that kidney transplantations are the most commonly performed transplants with well-defined measures of rejection and graft failure, this organs will be studied in a six-center study designed to accrue the target number of transplant recipients within the one-year study period. The study has now been branched off into 2 phases. Phase 1: consists of randomization of patients onto brand and generic tacrolimus. This was completed once 40 brand patients were enrolled. Phase 2: consists of patients being enrolled only on generic tacrolimus (standard of care from subject's insurance). This will be completed once there is a total of 160 generic participants. 200 participants total in the study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedAug 15, 2016
Enrollment StartMar 1, 2018
Primary CompletionJun 11, 2021
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 9.9 years ago

Interventions

Prografdrug

Brand Drug for the duration of the study.

Tacrolimusdrug

Generic