Mycophenolate Mofetil (MMF) in Patients With IgA Nephropathy
Stopped early · Phase 3 · Has a placebo group
Conditions studied: IgA Nephropathy
In brief
IgA nephropathy (IgAN) is the most common type of glomerulonephritis worldwide. 15-40% of individuals diagnosed with IgAN, including children, will eventually progress to chronic renal insufficiency (CRI) and end stage renal disease (ESRD). The study is to evaluate the safety and benefits of MMF in patients with IgAN who have been pre-treated (and continue to be treated) with angiotensin converting enzyme inhibitors (ACEi) and fish oil supplements (FOS).
Key facts
- Study ID
- NCT00318474
- Run by
- St. Joseph's Hospital and Medical Center, Phoenix
- People needed
- 184
- Starts
- 2002-01-01
- Expected to finish
- 2010-03-01
- Last updated by the study team
- 2016-03-07
Who can join
Age: 7 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients ages 7-70 years old
- Renal biopsy, diagnostic for IgA nephropathy
- Must be able to take oral medication
You may not qualify if…
- Clinical and histologic evidence of systemic lupus erythematosus
- Well-documented history of Henoch-Schonlein purpura.
- Clinical evidence of cirrhosis or chronic liver disease
- Abnormal laboratory values at the time of study entry
- Estimated GFR outside of protocol defined limits
- History of significant gastrointestinal disorder
- Active systemic infection or history of serious infection within one month of entry or known infection with HIV, hepatitis B, or hepatitis C.
- Other major organ system disease or malignancy
- Current or prior treatment with MMF or azathioprine
Where it is running
- St. Joseph's Hospital and Medical Center — Phoenix, Arizona, United States
Full record on ClinicalTrials.gov
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