Clinical trial

Mycophenolate Mofetil in Membranous Nephropathy

NCT00135967 · Radboud University Medical Center, Other · Completed

Key facts

NCT number NCT00135967
Title Mycophenolate Mofetil in Membranous Nephropathy
Official title Treatment of Patients With Membranous Nephropathy and Renal Insufficiency With Mycophenolate Mofetil and Prednisone: a Pilot Study
Lead sponsor Radboud University Medical Center, Other
Collaborators Hoffmann-La Roche Industry
Status Completed
Phase Phase 2/Phase 3
Study type Interventional
Conditions Glomerulonephritis, Membranous
Intervention type Drug
Interventions mycophenolate mofetil orally 1000 mg twice a day (BID), prednisone 0, 5 mg/kg orally on alternate days, intravenous (i.v.) methylprednisolone 1000 mg, total 9
Enrollment 30
Start date May 1, 2002
First posted Aug 26, 2005
Last update posted Dec 6, 2005
Countries Netherlands

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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