A Study of Mycophenolate Mofetil (CellCept) in Management of Patients With Lupus Nephritis.
Lupus Nephritis
About this trial
This is an interventional treatment trial for Lupus Nephritis
Eligibility Criteria
Inclusion Criteria:
- male or female patients, 12-75 years of age;
- diagnosis of systemic lupus erythematosus;
- kidney biopsy within 6 months of study, with histological diagnosis of lupus nephritis;
- laboratory evidence of active nephritis.
Exclusion Criteria:
- continuous dialysis starting >2 weeks before randomization into induction phase, and/or with an anticipated duration of >8 weeks;
- previous or planned kidney transplant;
- other clinically significant active medical conditions.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Active Comparator
Experimental
Active Comparator
Induction Phase: Mycophenolate mofetil
Induction Phase: Cyclophosphamide
Maintenance Phase: Mycophenolate mofetil
Maintenance Phase: Azathioprine
Participants received oral mycophenolate mofetil (MMF) 1.5 g twice a day and concomitant corticosteroids for the 24 weeks of the Induction Phase.
Participants received monthly infusions of cyclophosphamide, 0.5 to 1.0 g per square meter of body surface area and concomitant treatment with corticosteroids for the 24 week Induction Phase.
Participants received mycophenolate mofetil (MMF) 1.0 g orally twice a day, placebo to azathioprine orally once a day and corticosteroid for the 36 weeks Maintenance Phase.
Participants received azathioprine (AZA) 2 mg/kg/day orally once a day, placebo to mycophenolate mofetil orally twice a day and corticosteroid for the 36 weeks Maintenance Phase.