drugset / Trial / NCT02058875

Cardiovascular Risk Following Conversion to Full Dose Myfortic® and Neoral® Two-hour Post Level Monitoring

NCT02058875 ↗

Phase 4 Withdrawn University of Saskatchewan
RandomizedFactorialOpen-labelTreatment

Summary

The overall goal of this study is to improve cardiovascular outcomes in transplant recipients. The current standard immunosuppressive regimen in kidney transplant recipients depends on a higher exposure to the Calcineurin Inhibitor (CNI), and often a less than optimal dosage the of mycophenolic acid (MPA) derivative. The premise of this study is to investigate the effects of reversing this paradigm. More specifically, the effect of using maximum MPA dosages (in the form of enteric-coated mycophenolate sodium \[EC-MPS\] or Myfortic®) along with judicious CNI exposure (cyclosporine/Neoral®) will be investigated.

Timeline

Start
2014-02
Primary completion
2015-10
Completion
2015-10

Outcome

Outcome not reported

Stopped (Business): “The study funder retracted their grant funding offer before contract signed.”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclosporine Peptide — —
Comparator Mycophenolate Mofetil Small molecule — —
Subject mycophenolic acid Small molecule 1440 mg —
Comparator Prednisone Other / unclassified — —