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Study to Compare the Efficacy and Safety After Conversion to RaparoBell® or My-Rept® in Kidney Transplant Patients

Kidney Transplantation Clinical Trial

Official title:
Multi-center, Open-label, Randomized Controlled Phase 4 Study to Compare the Efficacy and Safety After Conversion to RaparoBell® or My-Rept® in Kidney Transplant Patients Undergoing Maintenance Therapy With CNI Plus MPA.[CORAL Study]

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and Safety after conversion to RaparoBell® or Myrept® in patients who in renal transplant patients undergoing maintenance therapy with Mycophenolic acid.

Clinical Trial Description

This study is a multi-center, Randomized, Open-label and phase IV clinical trial that evaluates the efficacy and safety after conversion to RaparoBell® or Myrept® administration for 24 weeks in renal transplant patients undergoing maintenance therapy with Mycophenolic acid. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05193565
Study type Interventional
Source Chong Kun Dang Pharmaceutical
Contact Chul Woo Yang, Ph.D
Phone 82-2-2258-6037
Email yangch@catholic.ac.kr
Status Recruiting
Phase Phase 4
Start date November 19, 2021
Completion date June 2024
View Details
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