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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT00377637




Registration number
NCT00377637
Ethics application status
Date submitted
15/09/2006
Date registered
18/09/2006
Date last updated
6/12/2011

Titles & IDs
Public title
A Study of Mycophenolate Mofetil (CellCept) in Management of Patients With Lupus Nephritis.
Scientific title
A Prospective, Randomized, Active Controlled, Parallel Group, Multi-center Trial to Assess the Efficacy and Safety of Mycophenolate Mofetil (MMF) in Inducing Response and Maintaining Remission in Subjects With Lupus Nephritis.
Secondary ID [1] 0 0
WX17801
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Lupus Nephritis 0 0
Condition category
Condition code
Renal and Urogenital 0 0 0 0
Other renal and urogenital disorders
Inflammatory and Immune System 0 0 0 0
Other inflammatory or immune system disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Mycophenolate mofetil (MMF)
Treatment: Drugs - Cyclophosphamide
Treatment: Drugs - Azathioprine
Treatment: Drugs - Placebo to Azathioprine
Treatment: Drugs - Placebo to Mycophenolate mofetil
Treatment: Drugs - Corticosteroid

Experimental: Induction Phase: Mycophenolate mofetil - Participants received oral mycophenolate mofetil (MMF) 1.5 g twice a day and concomitant corticosteroids for the 24 weeks of the Induction Phase.

Active comparator: Induction Phase: Cyclophosphamide - 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.

Experimental: Maintenance Phase: Mycophenolate mofetil - 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.

Active comparator: Maintenance Phase: Azathioprine - 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.


Treatment: Drugs: Mycophenolate mofetil (MMF)
Supplied as 500 mg tablets taken orally twice a day (BID). Dose specific for each arm. Dosing started at 500 mg BID for the first week, increasing by 500 mg in subsequent weeks until the final target dose was reached.

Treatment: Drugs: Cyclophosphamide
Intravenous cyclophosphamide (IVC) was administered every four weeks (monthly) to a total of six infusions.

Dosing was started at 0.75 g/m\^2 of body surface area for the first month, with subsequent doses at 0.5-1.0 g/m\^2. The target dose was 1.0 g/m\^2, but doses were titrated by 0.25 g/m\^2 increments to maintain nadir leukocyte count between 2500-4000/mm\^3.

Treatment: Drugs: Azathioprine
2 mg/kg/day orally, provided as 50 mg capsules to be taken after meals.

Treatment: Drugs: Placebo to Azathioprine
Placebo capsules matching Azathioprine taken orally once a day.

Treatment: Drugs: Placebo to Mycophenolate mofetil
Placebo tablets matching Mycophenolate mofetil taken orally twice daily.

Treatment: Drugs: Corticosteroid
Oral prednisolone (or equivalent) starting at a dose of 0.75-1.0 mg/kg/day (maximum 60 mg/day) tapered to 10 mg/day.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Induction Phase: Number of Patients Showing Treatment Response
Timepoint [1] 0 0
24 weeks
Primary outcome [2] 0 0
Maintenance Phase: Kaplan-Meier Estimates of Percentage of Participants Treatment Failure Free, by Time Interval
Timepoint [2] 0 0
From the start of the Maintenance Phase to Month 36
Secondary outcome [1] 0 0
Induction Phase: Number of Participants Achieving Complete Remission
Timepoint [1] 0 0
24 weeks
Secondary outcome [2] 0 0
Induction Phase: Change From Baseline to Week 24 in Serum Creatinine
Timepoint [2] 0 0
Baseline, Week 24
Secondary outcome [3] 0 0
Induction Phase: Change From Baseline to Week 24 in 24-hour Urine Protein
Timepoint [3] 0 0
Baseline, Week 24
Secondary outcome [4] 0 0
Induction Phase: Change From Baseline to Week 24 in Serum Albumin
Timepoint [4] 0 0
Baseline, Week 24
Secondary outcome [5] 0 0
Induction Phase: Change in Renal British Isles Lupus Assessment Group (BILAG) Score
Timepoint [5] 0 0
Baseline, 24 weeks
Secondary outcome [6] 0 0
Induction Phase: Change From Baseline in Short-Form Health Survey (SF-36) Domain and Component Scores
Timepoint [6] 0 0
Baseline and 24 weeks
Secondary outcome [7] 0 0
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Deaths
Timepoint [7] 0 0
From the start of the Maintenance Phase to Month 36
Secondary outcome [8] 0 0
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Participants With End-stage Renal Disease (ESRD)
Timepoint [8] 0 0
From the start of the Maintenance Phase to Month 36
Secondary outcome [9] 0 0
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Participants With Sustained Doubling of Serum Creatinine
Timepoint [9] 0 0
From the start of the Maintenance Phase to Month 36
Secondary outcome [10] 0 0
Maintenance Phase: Events Contributing to the Primary Endpoint: Kaplan-Meier Estimates of Percentage of Participants Renal Flare Free, by Time Interval
Timepoint [10] 0 0
From the start of the Maintenance Phase to Month 36
Secondary outcome [11] 0 0
Maintenance Phase: Events Contributing to the Primary Endpoint: Kaplan-Meier Estimates of Percentage of Participants Not Receiving Rescue Therapy
Timepoint [11] 0 0
From the start of the Maintenance Phase to Month 36
Secondary outcome [12] 0 0
Maintenance Phase: Participants With Major Extra-renal Flare
Timepoint [12] 0 0
From the start of the Maintenance Phase to Month 36

Eligibility
Key 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.
Minimum age
12 Years
Maximum age
75 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key 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.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/07/2005
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/03/2010
Sample size
Target
Accrual to date
Final
370
Recruitment in Australia
Recruitment state(s)
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- Adelaide
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- Camperdown
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- Melbourne
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- Parkville
Recruitment hospital [5] 0 0
- Woodville
Recruitment postcode(s) [1] 0 0
SA 5000 - Adelaide
Recruitment postcode(s) [2] 0 0
2050 - Camperdown
Recruitment postcode(s) [3] 0 0
3168 - Melbourne
Recruitment postcode(s) [4] 0 0
3052 - Parkville
Recruitment postcode(s) [5] 0 0
5011 - Woodville
Recruitment outside Australia
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Hoffmann-La Roche
Address
Country
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Commercial sector/industry
Name [1] 0 0
Aspreva Pharmaceuticals
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Clinical Trials
Address 0 0
Hoffmann-La Roche
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results are available at https://clinicaltrials.gov/study/NCT00377637