Clinical Trials Directory

Trials / Completed

CompletedNCT01842269

Evaluate the Efficacy and Safety of My-Rept® Tablet vs. My-Rept® Capsule in Combination With Tacrolimus in Kidney Transplant Patients

Open Label, Randomized, Multi-center, Phase 4 Trial to Evaluate the Efficacy and Safety of My-Rept® Tablet(Mycophenolate Mofetil 500mg/Tab.) Versus My-Rept® Capsule(Mycophenolate Mofetil 250mg/Cap.) in Combination With Tacrolimus for 26 Weeks in Kidney Transplant Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
156 (actual)
Sponsor
Chong Kun Dang Pharmaceutical · Industry
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

Efficacy and Safety of My-Rept® Tablet(Mycophenolate Mofetil 500mg/Tab.) versus My-Rept® Capsule(Mycophenolate Mofetil 250mg/Cap.) in Combination with Tacrolimus in Kidney Transplant Patients

Conditions

Interventions

TypeNameDescription
DRUGMycophenolate Mofetil 500mg
DRUGMycophenolate Mofetil 250mg

Timeline

Start date
2013-01-01
Primary completion
2015-04-01
Completion
2015-04-01
First posted
2013-04-29
Last updated
2015-08-19

Locations

11 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01842269. Inclusion in this directory is not an endorsement.

Evaluate the Efficacy and Safety of My-Rept® Tablet vs. My-Rept® Capsule in Combination With Tacrolimus in Kidney Transp (NCT01842269) · Clinical Trials Directory