drugset / Trial / NCT02161237

Asian Study to Investigate Safety and Efficacy of Optimized Dosing of Advagraf in Kidney Transplantation

NCT02161237 ↗

Phase 4 Completed 73 enrolled Astellas Pharma Inc
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary purpose of this study is to compare renal function between subjects receiving optimized dose Advagraf® over 52 weeks after kidney transplantation and subjects receiving standard dose Advagraf®. Pilot results of safety and efficacy in optimized dose Advagraf® over 52 weeks after kidney transplantation will also be obtained.

Timeline

Start
2014-06-26
Primary completion
2016-12-22
Completion
2016-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Tacrolimus Small molecule — Oral

Indications

No indication recorded.