Mycophenolate Mofetil (MMF) in Patients With IgA Nephropathy (IgAN)

Status Completed

Clinical Trial Summary

A multi-center, randomized, controlled clinical trial to evaluate the short-term and long-term efficacy and safety of mycophenolate mofetil (MMF) in reducing proteinuria and preserving renal function in patients with IgAN who have pre-treated (and continue to be treated) with angiotensin II receptor blockers (ARB), compared to the corticosteroids.

Clinical Trial Description

There are four phases of study for each subject. Phase 1 the screening phase. During this phase each potential subject will be evaluated to determine if he/she is eligible for the study.

Phase 2 the ARB lead-in phase will last for three months. Phase 3 the intervention phase. Each subject will be randomly received 12 months treatment with the study drugs (MMF, prednisone or MMF plus prednisone) Phase 4 following-up phase. All the patients will be followed by 3 years after study drug stopped. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00657059
Study type	Interventional
Source	Sun Yat-sen University
Contact
Status	Completed
Phase	Phase 3
Start date	September 2007
Completion date	May 2019

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See also
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