drugset / Trial / NCT00404833

Mycophenolate Mofetil in Membranous Nephropathy and Focal Segmental

NCT00404833

RandomizedParallel-groupOpen-labelTreatment

Summary

This is a prospective randomized open-label pilot study to investigate the effect of mycophenolate mofetil treatment in patients with abnormal urine protein excretion due to membranous nephropathy (MN) or focal segmental glomerulosclerosis (FSGS). The change in urine protein excretion will be the primary outcome studied. The treatment regimen comprising prednisolone and mycophenolate mofetil will be compared with prednisolone and chlorambucil in MN, and compared with prednisolone in FSGS. The study duration will be 12 months for each patient.

Timeline

Start
2003-01
Primary completion
Completion
2006-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Chlorambucil Other / unclassified
Subject Mycophenolate Mofetil Small molecule
Background Prednisolone Other / unclassified