Induction Treatment of Proliferative Lupus Nephritis With Leflunomide Combined With Prednisone
Primary Purpose
Nephritis, Lupus
Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
leflunomide combined with prednisone
Sponsored by
About this trial
This is an interventional treatment trial for Nephritis, Lupus
Eligibility Criteria
Inclusion Criteria: All patients were diagnosed as SLE according to the updated criteria of American College of Rheumatology in 1997, had a systemic lupus erythematosus disease activity index (SLEDAI)equal or greater than 8; had evident renal diseases and biopsy-documented diffuse proliferative or focal proliferative lupus nephritis, with or without coincident membranous nephropathy, and pathological activity index (AI)equal or greater than 4 Exclusion Criteria: Patients who had received cyclophosphamide within the previous 3 months, cerebral lupus, severe infection, liver disease, pregnancy, and anticipated poor compliance with the protocol.
Sites / Locations
- Renal Division, Peking University First Hospital
- Department of Nephrology, Kidney Center and key Lab of PLA, Chinese General Hospital of PLA
- Division of Nephrology, Nanfang Hospital, Southern Medical University
- Renal Division, the First Affiliated Hospital, Sun Yat-sen University
- Department of Rheumatology, the Second Affiliated Hospital, Harbin Medical University
- Department of Nephrology, Shanghai Changzheng Hospital
- Renal Division, Huashan Hospital, Fudan University
- Renal Division, Renji Hospital, Shanghai Jiaotong University
Outcomes
Primary Outcome Measures
complete remission of renal disease at 6 months
Secondary Outcome Measures
partial remission at 6 months and adverse events
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00268567
Brief Title
Induction Treatment of Proliferative Lupus Nephritis With Leflunomide Combined With Prednisone
Official Title
Phase 3 Study of Leflunomide Combined With Prednisone Treatment of Proliferative Lupus Nephritis as Induction Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
October 2004
Overall Recruitment Status
Completed
Study Start Date
October 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Peking University
4. Oversight
5. Study Description
Brief Summary
lupus nephritis accounts for the most morbidity and mortality in patients with SLE. Glucocorticoids combined with cyclophosphamide (CYC) are effective for the treatment of patients with proliferative lupus nephritis and have been the immunosuppressive regimen of choice for many years. However, some patients do not respond well to the regimen, and adverse effects of cyclophosphamide limit its use in certain patients. Leflunomide is a novel immunosuppressive agent currently used in the treatment of rheumatoid arthritis.There were a few pilot observational studies and reports suggesting leflunomide was also safe, well-tolerated and may be effective in SLE patients without important organ involvement. It has not been shown if leflunomide can be used in the treatment of patients with lupus nephritis. We therefore undertook a multi-center, controlled study to investigate the efficacy and safety profile of leflunomide compared with cyclophosphamide in the treatment of patients with biopsy proven proliferative lupus nephritis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nephritis, Lupus
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
leflunomide combined with prednisone
Primary Outcome Measure Information:
Title
complete remission of renal disease at 6 months
Secondary Outcome Measure Information:
Title
partial remission at 6 months and adverse events
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients were diagnosed as SLE according to the updated criteria of American College of Rheumatology in 1997, had a systemic lupus erythematosus disease activity index (SLEDAI)equal or greater than 8; had evident renal diseases and biopsy-documented diffuse proliferative or focal proliferative lupus nephritis, with or without coincident membranous nephropathy, and pathological activity index (AI)equal or greater than 4
Exclusion Criteria:
Patients who had received cyclophosphamide within the previous 3 months, cerebral lupus, severe infection, liver disease, pregnancy, and anticipated poor compliance with the protocol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Haiyan Wang, M.D.
Organizational Affiliation
Institute of Nephrology, Peking University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Renal Division, Peking University First Hospital
City
Beijing
ZIP/Postal Code
100034
Country
China
Facility Name
Department of Nephrology, Kidney Center and key Lab of PLA, Chinese General Hospital of PLA
City
Beijing
Country
China
Facility Name
Division of Nephrology, Nanfang Hospital, Southern Medical University
City
Guangzhou
Country
China
Facility Name
Renal Division, the First Affiliated Hospital, Sun Yat-sen University
City
Guangzhou
Country
China
Facility Name
Department of Rheumatology, the Second Affiliated Hospital, Harbin Medical University
City
Harbin
Country
China
Facility Name
Department of Nephrology, Shanghai Changzheng Hospital
City
Shanghai
Country
China
Facility Name
Renal Division, Huashan Hospital, Fudan University
City
Shanghai
Country
China
Facility Name
Renal Division, Renji Hospital, Shanghai Jiaotong University
City
Shanghai
Country
China
12. IPD Sharing Statement
Learn more about this trial
Induction Treatment of Proliferative Lupus Nephritis With Leflunomide Combined With Prednisone
We'll reach out to this number within 24 hrs