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A Study of Mycophenolate Mofetil (CellCept) in Management of Patients With Lupus Nephritis.

Primary Purpose

Lupus Nephritis

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Mycophenolate mofetil (MMF)
Cyclophosphamide
Azathioprine
Placebo to Azathioprine
Placebo to Mycophenolate mofetil
Corticosteroid
Sponsored by
Hoffmann-La Roche
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lupus Nephritis

Eligibility Criteria

12 Years - 75 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

Induction Phase: Mycophenolate mofetil

Induction Phase: Cyclophosphamide

Maintenance Phase: Mycophenolate mofetil

Maintenance Phase: Azathioprine

Arm Description

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.

Outcomes

Primary Outcome Measures

Induction Phase: Number of Patients Showing Treatment Response
Treatment response was adjudicated by a blinded clinical endpoints committee (CEC) and defined as: a) Decrease in proteinuria, defined as a decrease in the urine protein to creatinine ratio (UPCr) to <3 in subjects with baseline proteinuria ≥3 UPCr or a decrease in the UPCr by ≥50% in subjects with proteinuria <3 UPCr at Baseline, and b) Stabilization of serum creatinine or improvement. UPCr were derived from the 24 hour urine collection. Patients who did not show a treatment response at Week 24 or who withdrew earlier than Week 24 were considered non-responders.
Maintenance Phase: Kaplan-Meier Estimates of Percentage of Participants Treatment Failure Free, by Time Interval
Treatment Failure was adjudicated by a clinical endpoints committee and was defined as the time to the earliest occurrence of any one of the following: death, end stage renal disease, sustained doubling of serum creatinine, renal flare, or a requirement for rescue therapy for exacerbation or deterioration of Lupus nephritis. Kaplan-Meier survival curves were estimated from the observed time to treatment failure for each patient. The data presented are the percentage of participants who were treatment-failure free at each time interval as estimated by Kaplan-Meier.

Secondary Outcome Measures

Induction Phase: Number of Participants Achieving Complete Remission
Number of participants achieving complete remission as defined by return to normal serum creatinine, proteinuria ≤500 mg/24 hours and an inactive urinary sediment (absence of red blood cells, white blood cells or cellular or granular casts) after 24 weeks.
Induction Phase: Change From Baseline to Week 24 in Serum Creatinine
Induction Phase: Change From Baseline to Week 24 in 24-hour Urine Protein
24-hour urine protein was measured at Baseline and Week 24.
Induction Phase: Change From Baseline to Week 24 in Serum Albumin
Induction Phase: Change in Renal British Isles Lupus Assessment Group (BILAG) Score
BILAG indices provide a scoring system for the assessment of lupus disease activity in terms of the need for steroid treatment in 8 organs/systems. Eighty-six items were scored resulting in a classification of A (severe activity), B (moderate activity), C (mild activity), D (no current activity) and E (no activity ever observed) for each organ system. The BILAG individual system summaries were calculated by a program supplied by ADS-Limathon (Sheffield, UK). The score at baseline was compared to the score at the 24 week endpoint for each treatment group, reported here for the renal system.
Induction Phase: Change From Baseline in Short-Form Health Survey (SF-36) Domain and Component Scores
The SF-36 is a 36 item quality of life questionnaire. The short-form version has eleven questions that permit the participant to rate how they feel that particular day. The SF-36 consists of eight scaled scores and two component scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 score with the higher scores indicating better quality of life.
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Deaths
Treatment Failure was adjudicated by a clinical endpoints committee (CEC) and was defined as the time to the earliest occurrence of any one of the following: death, end stage renal disease, sustained doubling of serum creatinine, renal flare, or a requirement for rescue therapy for exacerbation or deterioration of Lupus nephritis (LN).
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Participants With End-stage Renal Disease (ESRD)
Time to treatment failure, adjudicated by the Clinical Endpoints Committee (CEC), was defined as any 1 the following: death, ESRD, sustained doubling of serum creatinine, renal flare (proteinuric or nephritic), or requirement for rescue therapy to treat deterioration or exacerbation of Lupus nephritis. ESRD is defined as progression to chronic hemodialysis or renal transplant.
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Participants With Sustained Doubling of Serum Creatinine
Sustained doubling of serum creatinine concentration is defined as the first serum creatinine value that is twice the mean of the lowest 2 values from screening to end of induction, as confirmed by a second serum creatinine value obtained at least 4 weeks after the initial doubling.
Maintenance Phase: Events Contributing to the Primary Endpoint: Kaplan-Meier Estimates of Percentage of Participants Renal Flare Free, by Time Interval
A proteinuric flare is defined as a doubling of the urine protein:creatinine ratio, and proteinuria ≥1 g/24 h in patients with urine protein ≤0.5 g/24 h at the end of the induction phase, or proteinuria ≥2 g/24 h if urine protein was >0.5 g/24 h at the end of the induction phase. A nephritic flare is defined as a 25% increase in serum creatinine accompanied by 1 or more of the following: (a) simultaneous doubling of the proteinuria reaching a minimum of 2 g/24 h (b) new/increased hematuria or (c) the appearance of cellular casts. All flares were adjudicated by a clinical endpoints committee.
Maintenance Phase: Events Contributing to the Primary Endpoint: Kaplan-Meier Estimates of Percentage of Participants Not Receiving Rescue Therapy
The primary efficacy parameter was the time to treatment failure, adjudicated by the Clinical Endpoints Committee (CEC), defined as any of the following: death, end stage renal disease, sustained doubling of serum creatinine, renal flare, or requirement for rescue therapy to treat deterioration or exacerbation of Lupus nephritis. Kaplan-Meier survival curves were estimated from the observed time to rescue treatment for each patient. The data presented are the percentage of participants who were rescue treatment free at each time interval as estimated by Kaplan-Meier.
Maintenance Phase: Participants With Major Extra-renal Flare
A major extra-renal flare is defined as a British Isles Lupus Assessment Group (BILAG) Score category A in one extrarenal organ or three organs with concurrent category B scores. BILAG indices provide a scoring system for the assessment of lupus disease activity in terms of the need for steroid treatment in 8 organs/systems. Eighty-six items were scored resulting in a classification of A (severe activity), B (moderate activity), C (mild activity), D (no current activity) and E (no activity ever observed) for each organ system.

Full Information

First Posted
September 15, 2006
Last Updated
October 31, 2011
Sponsor
Hoffmann-La Roche
Collaborators
Aspreva Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT00377637
Brief Title
A Study of Mycophenolate Mofetil (CellCept) in Management of Patients With Lupus Nephritis.
Official 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.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2011
Overall Recruitment Status
Completed
Study Start Date
July 2005 (undefined)
Primary Completion Date
March 2007 (Actual)
Study Completion Date
March 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hoffmann-La Roche
Collaborators
Aspreva Pharmaceuticals

4. Oversight

5. Study Description

Brief Summary
This 2 arm study assessed the efficacy of Mycophenolate Mofetil (MMF; CellCept) compared to cyclophosphamide in inducing a response in patients with lupus nephritis, and the long term efficacy of MMF compared to azathioprine in maintaining remission and renal function. Patients were randomized to receive either MMF (1.5 g twice daily [bid]) or cyclophosphamide (0.5-1.0 g/m^2 in monthly pulses) in the induction phase. Those patients meeting criteria for response were re-randomized for entry into the maintenance phase, to receive either MMF (1 g bid) or azathioprine (2 mg/kg/day).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lupus Nephritis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
370 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Induction Phase: Mycophenolate mofetil
Arm Type
Experimental
Arm Description
Participants received oral mycophenolate mofetil (MMF) 1.5 g twice a day and concomitant corticosteroids for the 24 weeks of the Induction Phase.
Arm Title
Induction Phase: Cyclophosphamide
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Maintenance Phase: Mycophenolate mofetil
Arm Type
Experimental
Arm Description
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.
Arm Title
Maintenance Phase: Azathioprine
Arm Type
Active Comparator
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Mycophenolate mofetil (MMF)
Other Intervention Name(s)
CellCept
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Other Intervention Name(s)
Endoxan®
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Azathioprine
Other Intervention Name(s)
Imuran®
Intervention Description
2 mg/kg/day orally, provided as 50 mg capsules to be taken after meals.
Intervention Type
Drug
Intervention Name(s)
Placebo to Azathioprine
Intervention Description
Placebo capsules matching Azathioprine taken orally once a day.
Intervention Type
Drug
Intervention Name(s)
Placebo to Mycophenolate mofetil
Intervention Description
Placebo tablets matching Mycophenolate mofetil taken orally twice daily.
Intervention Type
Drug
Intervention Name(s)
Corticosteroid
Intervention Description
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.
Primary Outcome Measure Information:
Title
Induction Phase: Number of Patients Showing Treatment Response
Description
Treatment response was adjudicated by a blinded clinical endpoints committee (CEC) and defined as: a) Decrease in proteinuria, defined as a decrease in the urine protein to creatinine ratio (UPCr) to <3 in subjects with baseline proteinuria ≥3 UPCr or a decrease in the UPCr by ≥50% in subjects with proteinuria <3 UPCr at Baseline, and b) Stabilization of serum creatinine or improvement. UPCr were derived from the 24 hour urine collection. Patients who did not show a treatment response at Week 24 or who withdrew earlier than Week 24 were considered non-responders.
Time Frame
24 weeks
Title
Maintenance Phase: Kaplan-Meier Estimates of Percentage of Participants Treatment Failure Free, by Time Interval
Description
Treatment Failure was adjudicated by a clinical endpoints committee and was defined as the time to the earliest occurrence of any one of the following: death, end stage renal disease, sustained doubling of serum creatinine, renal flare, or a requirement for rescue therapy for exacerbation or deterioration of Lupus nephritis. Kaplan-Meier survival curves were estimated from the observed time to treatment failure for each patient. The data presented are the percentage of participants who were treatment-failure free at each time interval as estimated by Kaplan-Meier.
Time Frame
From the start of the Maintenance Phase to Month 36
Secondary Outcome Measure Information:
Title
Induction Phase: Number of Participants Achieving Complete Remission
Description
Number of participants achieving complete remission as defined by return to normal serum creatinine, proteinuria ≤500 mg/24 hours and an inactive urinary sediment (absence of red blood cells, white blood cells or cellular or granular casts) after 24 weeks.
Time Frame
24 weeks
Title
Induction Phase: Change From Baseline to Week 24 in Serum Creatinine
Time Frame
Baseline, Week 24
Title
Induction Phase: Change From Baseline to Week 24 in 24-hour Urine Protein
Description
24-hour urine protein was measured at Baseline and Week 24.
Time Frame
Baseline, Week 24
Title
Induction Phase: Change From Baseline to Week 24 in Serum Albumin
Time Frame
Baseline, Week 24
Title
Induction Phase: Change in Renal British Isles Lupus Assessment Group (BILAG) Score
Description
BILAG indices provide a scoring system for the assessment of lupus disease activity in terms of the need for steroid treatment in 8 organs/systems. Eighty-six items were scored resulting in a classification of A (severe activity), B (moderate activity), C (mild activity), D (no current activity) and E (no activity ever observed) for each organ system. The BILAG individual system summaries were calculated by a program supplied by ADS-Limathon (Sheffield, UK). The score at baseline was compared to the score at the 24 week endpoint for each treatment group, reported here for the renal system.
Time Frame
Baseline, 24 weeks
Title
Induction Phase: Change From Baseline in Short-Form Health Survey (SF-36) Domain and Component Scores
Description
The SF-36 is a 36 item quality of life questionnaire. The short-form version has eleven questions that permit the participant to rate how they feel that particular day. The SF-36 consists of eight scaled scores and two component scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 score with the higher scores indicating better quality of life.
Time Frame
Baseline and 24 weeks
Title
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Deaths
Description
Treatment Failure was adjudicated by a clinical endpoints committee (CEC) and was defined as the time to the earliest occurrence of any one of the following: death, end stage renal disease, sustained doubling of serum creatinine, renal flare, or a requirement for rescue therapy for exacerbation or deterioration of Lupus nephritis (LN).
Time Frame
From the start of the Maintenance Phase to Month 36
Title
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Participants With End-stage Renal Disease (ESRD)
Description
Time to treatment failure, adjudicated by the Clinical Endpoints Committee (CEC), was defined as any 1 the following: death, ESRD, sustained doubling of serum creatinine, renal flare (proteinuric or nephritic), or requirement for rescue therapy to treat deterioration or exacerbation of Lupus nephritis. ESRD is defined as progression to chronic hemodialysis or renal transplant.
Time Frame
From the start of the Maintenance Phase to Month 36
Title
Maintenance Phase: Events Contributing to the Primary Endpoint: Number of Participants With Sustained Doubling of Serum Creatinine
Description
Sustained doubling of serum creatinine concentration is defined as the first serum creatinine value that is twice the mean of the lowest 2 values from screening to end of induction, as confirmed by a second serum creatinine value obtained at least 4 weeks after the initial doubling.
Time Frame
From the start of the Maintenance Phase to Month 36
Title
Maintenance Phase: Events Contributing to the Primary Endpoint: Kaplan-Meier Estimates of Percentage of Participants Renal Flare Free, by Time Interval
Description
A proteinuric flare is defined as a doubling of the urine protein:creatinine ratio, and proteinuria ≥1 g/24 h in patients with urine protein ≤0.5 g/24 h at the end of the induction phase, or proteinuria ≥2 g/24 h if urine protein was >0.5 g/24 h at the end of the induction phase. A nephritic flare is defined as a 25% increase in serum creatinine accompanied by 1 or more of the following: (a) simultaneous doubling of the proteinuria reaching a minimum of 2 g/24 h (b) new/increased hematuria or (c) the appearance of cellular casts. All flares were adjudicated by a clinical endpoints committee.
Time Frame
From the start of the Maintenance Phase to Month 36
Title
Maintenance Phase: Events Contributing to the Primary Endpoint: Kaplan-Meier Estimates of Percentage of Participants Not Receiving Rescue Therapy
Description
The primary efficacy parameter was the time to treatment failure, adjudicated by the Clinical Endpoints Committee (CEC), defined as any of the following: death, end stage renal disease, sustained doubling of serum creatinine, renal flare, or requirement for rescue therapy to treat deterioration or exacerbation of Lupus nephritis. Kaplan-Meier survival curves were estimated from the observed time to rescue treatment for each patient. The data presented are the percentage of participants who were rescue treatment free at each time interval as estimated by Kaplan-Meier.
Time Frame
From the start of the Maintenance Phase to Month 36
Title
Maintenance Phase: Participants With Major Extra-renal Flare
Description
A major extra-renal flare is defined as a British Isles Lupus Assessment Group (BILAG) Score category A in one extrarenal organ or three organs with concurrent category B scores. BILAG indices provide a scoring system for the assessment of lupus disease activity in terms of the need for steroid treatment in 8 organs/systems. Eighty-six items were scored resulting in a classification of A (severe activity), B (moderate activity), C (mild activity), D (no current activity) and E (no activity ever observed) for each organ system.
Time Frame
From the start of the Maintenance Phase to Month 36

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clinical Trials
Organizational Affiliation
Hoffmann-La Roche
Official's Role
Study Director
Facility Information:
City
Huntsville
State/Province
Alabama
ZIP/Postal Code
35801
Country
United States
City
La Jolla
State/Province
California
ZIP/Postal Code
92037
Country
United States
City
Los Angeles
State/Province
California
ZIP/Postal Code
90095
Country
United States
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
City
San Leandro
State/Province
California
ZIP/Postal Code
94578
Country
United States
City
Torrance
State/Province
California
ZIP/Postal Code
90502
Country
United States
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30303
Country
United States
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60637
Country
United States
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109-0358
Country
United States
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65212
Country
United States
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11203
Country
United States
City
Lake Success
State/Province
New York
ZIP/Postal Code
11042
Country
United States
City
New York
State/Province
New York
ZIP/Postal Code
10003
Country
United States
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599-7280
Country
United States
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44136
Country
United States
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
City
Charleston
State/Province
South Carolina
ZIP/Postal Code
29425
Country
United States
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
City
Buenos Aires
ZIP/Postal Code
C1015ABO
Country
Argentina
City
Buenos Aires
ZIP/Postal Code
C1425DQK
Country
Argentina
City
Córdoba
ZIP/Postal Code
5016
Country
Argentina
City
San Isidro
ZIP/Postal Code
B1602BPPD
Country
Argentina
City
Tucuman
ZIP/Postal Code
T4000AXL
Country
Argentina
City
Adelaide
ZIP/Postal Code
SA 5000
Country
Australia
City
Camperdown
ZIP/Postal Code
2050
Country
Australia
City
Melbourne
ZIP/Postal Code
3168
Country
Australia
City
Parkville
ZIP/Postal Code
3052
Country
Australia
City
Woodville
ZIP/Postal Code
5011
Country
Australia
City
Bruxelles
ZIP/Postal Code
1200
Country
Belgium
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
City
Liege
ZIP/Postal Code
4000
Country
Belgium
City
Rio de Janeiro
ZIP/Postal Code
20551-030
Country
Brazil
City
Sao Paulo
ZIP/Postal Code
04039-020
Country
Brazil
City
Sorocaba
ZIP/Postal Code
18030-210
Country
Brazil
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1L7
Country
Canada
City
Victoria
State/Province
British Columbia
ZIP/Postal Code
V8Z 7X8
Country
Canada
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 2Y9
Country
Canada
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 4V2
Country
Canada
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5T 2S8
Country
Canada
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H1T 2M4
Country
Canada
City
Beijing
ZIP/Postal Code
100034
Country
China
City
Guangdong
ZIP/Postal Code
510008
Country
China
City
Guangzhou
ZIP/Postal Code
510630
Country
China
City
Jiangsu
ZIP/Postal Code
210002
Country
China
City
Shanghai
ZIP/Postal Code
200001
Country
China
City
Brno
ZIP/Postal Code
656 91
Country
Czech Republic
City
Praha 2
ZIP/Postal Code
128 08
Country
Czech Republic
City
Lille
ZIP/Postal Code
59037
Country
France
City
Lyon
ZIP/Postal Code
69437
Country
France
City
Nantes
ZIP/Postal Code
44035
Country
France
City
Paris
ZIP/Postal Code
75679
Country
France
City
Paris
ZIP/Postal Code
75877
Country
France
City
Toulouse
ZIP/Postal Code
31059
Country
France
City
Aachen
ZIP/Postal Code
52074
Country
Germany
City
Bad Bramstedt
ZIP/Postal Code
24576
Country
Germany
City
Berlin
ZIP/Postal Code
10117
Country
Germany
City
Berlin
ZIP/Postal Code
14059
Country
Germany
City
Dresden
ZIP/Postal Code
01307
Country
Germany
City
Düsseldorf
ZIP/Postal Code
40225
Country
Germany
City
Erlangen
ZIP/Postal Code
91054
Country
Germany
City
Hannover
ZIP/Postal Code
30625
Country
Germany
City
Leipzig
ZIP/Postal Code
04103
Country
Germany
City
Muenster
ZIP/Postal Code
48149
Country
Germany
City
München
ZIP/Postal Code
80336
Country
Germany
City
München
ZIP/Postal Code
81675
Country
Germany
City
Athens
ZIP/Postal Code
11521
Country
Greece
City
Athens
ZIP/Postal Code
11527
Country
Greece
City
Heraklion
ZIP/Postal Code
71500
Country
Greece
City
Debrecen
ZIP/Postal Code
4032
Country
Hungary
City
Pécs
ZIP/Postal Code
7632
Country
Hungary
City
Szeged
ZIP/Postal Code
2724
Country
Hungary
City
Brescia
ZIP/Postal Code
25125
Country
Italy
City
Milano
ZIP/Postal Code
20149
Country
Italy
City
Padova
ZIP/Postal Code
35128
Country
Italy
City
Pisa
ZIP/Postal Code
56100
Country
Italy
City
Udine
ZIP/Postal Code
33100
Country
Italy
City
Merida
ZIP/Postal Code
97000
Country
Mexico
City
Mexico City
ZIP/Postal Code
14000
Country
Mexico
City
San Luis Potosi
ZIP/Postal Code
78240
Country
Mexico
City
Lisboa
Country
Portugal
City
Porto
ZIP/Postal Code
4200-319
Country
Portugal
City
Alicante
ZIP/Postal Code
03010
Country
Spain
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
City
Barcelona
ZIP/Postal Code
08036
Country
Spain
City
Madrid
ZIP/Postal Code
28041
Country
Spain
City
Malaga
ZIP/Postal Code
29010
Country
Spain
City
Santander
ZIP/Postal Code
39008
Country
Spain
City
Sevilla
ZIP/Postal Code
41013
Country
Spain
City
Birmingham
ZIP/Postal Code
B15 2TT
Country
United Kingdom
City
Cambridge
ZIP/Postal Code
CB2 2QQ
Country
United Kingdom
City
Leeds
ZIP/Postal Code
LS1 3EX
Country
United Kingdom
City
London
ZIP/Postal Code
SE1 7EH
Country
United Kingdom
City
London
ZIP/Postal Code
W12 OHS
Country
United Kingdom
City
London
ZIP/Postal Code
WIT 4NJ
Country
United Kingdom
City
Manchester
ZIP/Postal Code
M13 9WL
Country
United Kingdom
City
Newcastle Upon Tyne
ZIP/Postal Code
NE7 7DN
Country
United Kingdom
City
Sheffield
ZIP/Postal Code
S10 2JF
Country
United Kingdom
City
Southampton
ZIP/Postal Code
SO16 6YD
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
22922564
Citation
Sundel R, Solomons N, Lisk L; Aspreva Lupus Management Study (ALMS) Group. Efficacy of mycophenolate mofetil in adolescent patients with lupus nephritis: evidence from a two-phase, prospective randomized trial. Lupus. 2012 Nov;21(13):1433-43. doi: 10.1177/0961203312458466. Epub 2012 Aug 24.
Results Reference
derived
PubMed Identifier
22087680
Citation
Dooley MA, Jayne D, Ginzler EM, Isenberg D, Olsen NJ, Wofsy D, Eitner F, Appel GB, Contreras G, Lisk L, Solomons N; ALMS Group. Mycophenolate versus azathioprine as maintenance therapy for lupus nephritis. N Engl J Med. 2011 Nov 17;365(20):1886-95. doi: 10.1056/NEJMoa1014460.
Results Reference
derived
PubMed Identifier
21080348
Citation
Dall'Era M, Stone D, Levesque V, Cisternas M, Wofsy D. Identification of biomarkers that predict response to treatment of lupus nephritis with mycophenolate mofetil or pulse cyclophosphamide. Arthritis Care Res (Hoboken). 2011 Mar;63(3):351-7. doi: 10.1002/acr.20397. Epub 2010 Nov 15.
Results Reference
derived
PubMed Identifier
20039429
Citation
Ginzler EM, Wofsy D, Isenberg D, Gordon C, Lisk L, Dooley MA; ALMS Group. Nonrenal disease activity following mycophenolate mofetil or intravenous cyclophosphamide as induction treatment for lupus nephritis: findings in a multicenter, prospective, randomized, open-label, parallel-group clinical trial. Arthritis Rheum. 2010 Jan;62(1):211-21. doi: 10.1002/art.25052. Erratum In: Arthritis Rheum. 2010 Oct;62(10):3005.
Results Reference
derived
PubMed Identifier
19933596
Citation
Isenberg D, Appel GB, Contreras G, Dooley MA, Ginzler EM, Jayne D, Sanchez-Guerrero J, Wofsy D, Yu X, Solomons N. Influence of race/ethnicity on response to lupus nephritis treatment: the ALMS study. Rheumatology (Oxford). 2010 Jan;49(1):128-40. doi: 10.1093/rheumatology/kep346. Epub 2009 Nov 20.
Results Reference
derived

Learn more about this trial

A Study of Mycophenolate Mofetil (CellCept) in Management of Patients With Lupus Nephritis.

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