drugset / Trial / NCT04763096

Evaluate the Efficacy and Safety of the ADVAGRAF®

NCT04763096 ↗

Phase 4 Completed 101 enrolled Linical Korea Asan Medical Center · collab
NaSingle-groupOpen-labelHealth-services research

Summary

The primary objective of this study is to evaluate the efficacy of 6-month treatment with Advagraf® converted from 12-month treatment with tacrolimus in stable liver transplant recipients. The secondary objective of this study is to evaluate severity of acute rejection confirmed by biopsy in 24 weeks, incidence of chronic rejection, patient and graft survival rates in 24 weeks, incidence of adverse events, blood pressure, tacrolimus trough level, drug compliance, and adherence.

Timeline

Start
2016-11
Primary completion
2020-04
Completion
2020-04

Outcome

Met primary endpoint

paper treatment difference 2.6%, 95% confidence interval -7.3%, 12.4%), falling within the predefined 15% noninferiority margin. PMID 20840481 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tacrolimus Small molecule — —

Indications

No indication recorded.