IgA Nephropathy Clinical Trial
Official title:
Multi-center, Randomized, Open Label, Comparative, Phase IV Study to Evaluate the Efficacy and Safety of a Combination of Mycophenolate Mofetil and Corticosteroid for 48 Weeks in Advanced IgA Nephropathy
The purpose of this clinical study is to evaluate the efficacy and safety of that test group was administered with Mycophenolate Mofetil in combination with corticosteroid in patients with advanced IgA nephropathy. The control group will be observed for up to 48 weeks without administration of Mycophenolate Mofetil.
The subject who signed the written agreement to participate in the clinical trial evaluates
the conformity and then 1: 1 randomly allocated.
The study group were taken 48 weeks with MYREPT ® capsules in combination with
corticosteroids and the control group were asked to preserve the conservative treatment
regimen prior to the clinical trial registration Maintenance.
The subject who started taking the study medicine will carry out the examination and
procedure if it has to be carried out for the visit via outpatient clinic at 4 weeks, 12
weeks, 24 weeks, 36 weeks, 48 weeks.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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