drugset / Trial / NCT06268769

Tacrolimus C:D Ratio Measured in Renal Transplant Recipients Treated With Once-daily Prolonged-release Drugs

NCT06268769

Phase 4 Recruiting 300 enrolled Edward Geissler Chiesi Pharmaceuticals GmbH · collab
RandomizedParallel-groupOpen-labelPrevention

Summary

The goal of this clinical trial is to compare the bioavailability and practicability of two different formulations of tacrolimus in kidney transplant recipients. The main objective is to demonstrate that Envarsus® (test drug) has superior (higher) oral bioavailability compared with Advagraf™ (comparator drug) at 12 weeks after kidney transplantation. The trial also aims to compare the practicability (handling) of the two drugs using a series of pharmacokinetic parameters and to explore the relationship between drug bioavailability and long-term clinical outcomes, with a special focus on dose-dependent adverse reactions, measured until 3 years post-transplantation. The trial incorporates a pharmacokinetic sub-study designed to profile the peak tacrolimus blood concentration up to 6 hours after drug intake on the day of the 12-week study visit.

Timeline

Start
2024-03-09
Primary completion
2026-12
Completion
2029-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Tacrolimus Small molecule Oral