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Trial registered on ANZCTR
Registration number
ACTRN12612000298819
Ethics application status
Approved
Date submitted
7/03/2012
Date registered
15/03/2012
Date last updated
15/03/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
A Study to Evaluate the Safety and Tolerability of Epratuzumab in Patients With Systemic Lupus Erythematosus.
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Scientific title
A phase 3, multicenter, open-label, extension study to assess the safety and tolerability of epratuzumab treatment in systemic lupus erythematosus subjects (EMBODY 4)
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Secondary ID [1]
273550
0
NCT01408576 Clintrials.gov
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Universal Trial Number (UTN)
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Trial acronym
EMBODY 4
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Systemic Lupus Erythematosus
265772
0
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Condition category
Condition code
Inflammatory and Immune System
265920
265920
0
0
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Autoimmune diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Epratuzumab 600mg intravenous infusions delivered once a week (QW) via slow infusion for a total of 4 consecutive weeks (cumulative dose (CMD) 2400mg) over eight 12-week treatment cycles
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Intervention code [1]
264508
0
Treatment: Drugs
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Comparator / control treatment
Not applicable
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
266681
0
The percentage of subjects meeting treatment response criteria at week 48 and week 96 according to a combined response index which incorporates criteria for achievement from the BILAG, SLEDAI, and physician's global assessment of disease activity.
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Assessment method [1]
266681
0
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Timepoint [1]
266681
0
week 48 and week 96
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Secondary outcome [1]
296552
0
The percentage of subjects meeting treatment response criteria at all other time points assessed during the study according to a combined response index which incorporates criteria for achievement from the BILAG, SLEDAI, and physician's global assessment of disease activity.
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Assessment method [1]
296552
0
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Timepoint [1]
296552
0
All other time points assessed during the study
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Eligibility
Key inclusion criteria
The subject has completed double-blind study SL0009 (ACTRN12611000464965) or SL0010, or the subject has terminated prematurely at Week 16 or later in SL0009 or SL0010 due to lack of efficacy, as described in the respective protocols and would, in the opinion of the investigator, continue to benefit from continued epratuzumab treatment in SL0012.
The subject has maintained the eligibility requirements (including concomitant medication restrictions) throughout their participation in the prior study
Woman of childbearing potential using an acceptable method of birth control
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Subject has active, severe, neuropsychiatric SLE, defined as any neuropsychiatric element scoring BILAG level A disease
Subject has active, severe, SLE disease activity which involves the renal system defined by BILAG renal level A activity
Evidence of an immunosuppressive state
Subjects with a history of chronic infections, including but not limited to subjects with concurrent acute or chronic viral hepatitis B or C
Subjects with substance abuse/dependence or other concurrent medical conditions
Subjects with significant hematologic abnormalities
History of malignant cancer
Subject has used the prohibited medications
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Subjects who complete the Phase 3, double-blind, placebo-controlled study, SL0009, or terminate prematurely (at Week 16 or later) due to lack of efficacy, are eligible to enroll in this open-label extension study.
To enroll a subject (Visit 1), the investigator will call the IVRS and provide brief details about the subject to be enrolled. Each subject will keep the subject number assigned at Screening in SL0009, which serves as the subject identifier throughout SL0012. All subjects will receive epratuzumab 600mg infusions delivered QW for a total of 4 consecutive weeks (CMD 2400mg) repeated every 12 weeks.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
This study is open label and all subjects receive the same treatment. The interactive voice response system (IVRS) is responsible for issuing subject kits of epratuzumab, as appropriate, according to the visit schedule.
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 3
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
20/07/2011
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
1400
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment postcode(s) [1]
3966
0
3145
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Recruitment postcode(s) [2]
3967
0
3168
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Recruitment postcode(s) [3]
3968
0
4558
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Recruitment postcode(s) [4]
3969
0
2050
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Recruitment outside Australia
Country [1]
3499
0
Belgium
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State/province [1]
3499
0
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Country [2]
3500
0
Brazil
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State/province [2]
3500
0
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Country [3]
3501
0
Bulgaria
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State/province [3]
3501
0
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Country [4]
3502
0
Canada
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State/province [4]
3502
0
British Columbia
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Country [5]
3503
0
Canada
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State/province [5]
3503
0
Ontario
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Country [6]
3504
0
Canada
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State/province [6]
3504
0
Quebec
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Country [7]
3505
0
Czech Republic
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State/province [7]
3505
0
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Country [8]
3506
0
France
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State/province [8]
3506
0
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Country [9]
3507
0
Germany
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State/province [9]
3507
0
Baden-Wurttemberg
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Country [10]
3508
0
Hungary
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State/province [10]
3508
0
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Country [11]
3509
0
India
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State/province [11]
3509
0
Karnataka
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Country [12]
3510
0
Israel
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State/province [12]
3510
0
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Country [13]
3511
0
Italy
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State/province [13]
3511
0
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Country [14]
3512
0
Korea, Democratic People's Republic Of
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State/province [14]
3512
0
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Country [15]
3513
0
Mexico
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State/province [15]
3513
0
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Country [16]
3514
0
Netherlands
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State/province [16]
3514
0
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Country [17]
3515
0
Poland
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State/province [17]
3515
0
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Country [18]
3516
0
Romania
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State/province [18]
3516
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Country [19]
3517
0
Russian Federation
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State/province [19]
3517
0
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Country [20]
3518
0
South Africa
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State/province [20]
3518
0
Western Cape Province
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Country [21]
3519
0
Spain
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State/province [21]
3519
0
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Country [22]
3520
0
Taiwan, Province Of China
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State/province [22]
3520
0
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Country [23]
3521
0
Ukraine
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State/province [23]
3521
0
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Country [24]
3522
0
United Kingdom
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State/province [24]
3522
0
Essex
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Country [25]
3523
0
United Kingdom
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State/province [25]
3523
0
South Yorkshire
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Country [26]
3524
0
United Kingdom
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State/province [26]
3524
0
West Yorkshire
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Country [27]
3525
0
United Kingdom
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State/province [27]
3525
0
East Sussex
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Country [28]
3526
0
United Kingdom
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State/province [28]
3526
0
London
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Country [29]
3527
0
United Kingdom
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State/province [29]
3527
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West Midlands
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Country [30]
3528
0
United Kingdom
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State/province [30]
3528
0
Dorset
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Country [31]
3529
0
United States of America
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State/province [31]
3529
0
Alabama
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Country [32]
3530
0
United States of America
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State/province [32]
3530
0
Arkansas
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Country [33]
3531
0
United States of America
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State/province [33]
3531
0
California
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Country [34]
3532
0
United States of America
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State/province [34]
3532
0
Colorado
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Country [35]
3533
0
United States of America
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State/province [35]
3533
0
Connecticut
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Country [36]
3534
0
United States of America
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State/province [36]
3534
0
Florida
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Country [37]
3535
0
United States of America
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State/province [37]
3535
0
Georgia
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Country [38]
3536
0
United States of America
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State/province [38]
3536
0
Illinois
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Country [39]
3537
0
United States of America
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State/province [39]
3537
0
Kentucky
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Country [40]
3538
0
United States of America
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State/province [40]
3538
0
Louisiana
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Country [41]
3539
0
United States of America
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State/province [41]
3539
0
Maryland
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Country [42]
3540
0
United States of America
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State/province [42]
3540
0
Michigan
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Country [43]
3541
0
United States of America
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State/province [43]
3541
0
Minnesota
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Country [44]
3542
0
United States of America
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State/province [44]
3542
0
Missouri
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Country [45]
3543
0
United States of America
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State/province [45]
3543
0
New York
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Country [46]
3544
0
United States of America
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State/province [46]
3544
0
North Carolina
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Country [47]
3545
0
United States of America
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State/province [47]
3545
0
North Dakota
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Country [48]
3546
0
United States of America
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State/province [48]
3546
0
Ohio
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Country [49]
3547
0
United States of America
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State/province [49]
3547
0
Oklahoma
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Country [50]
3548
0
United States of America
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State/province [50]
3548
0
Oregon
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Country [51]
3549
0
United States of America
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State/province [51]
3549
0
Pennsylvania
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Country [52]
3550
0
United States of America
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State/province [52]
3550
0
South Carolina
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Country [53]
3551
0
United States of America
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State/province [53]
3551
0
Tennessee
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Country [54]
3552
0
United States of America
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State/province [54]
3552
0
Texas
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Country [55]
3553
0
United States of America
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State/province [55]
3553
0
Virginia
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Country [56]
3554
0
United States of America
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State/province [56]
3554
0
Washington
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Country [57]
3555
0
United States of America
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State/province [57]
3555
0
West Virginia
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Country [58]
3556
0
India
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State/province [58]
3556
0
Uttar Pradesh
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Country [59]
3557
0
India
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State/province [59]
3557
0
Lucknow
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Country [60]
3558
0
India
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State/province [60]
3558
0
Andhra Pradesh
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Country [61]
3559
0
Germany
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State/province [61]
3559
0
Nordrhein-Westfalen
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Country [62]
3560
0
Germany
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State/province [62]
3560
0
Sachsen
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Country [63]
3561
0
Germany
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State/province [63]
3561
0
Berlin
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Country [64]
3562
0
Germany
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State/province [64]
3562
0
Niedersachsen
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Country [65]
3563
0
Germany
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State/province [65]
3563
0
Hessen
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Country [66]
3564
0
South Africa
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State/province [66]
3564
0
Kwa-Zulu Natal
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Country [67]
3565
0
Puerto Rico
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State/province [67]
3565
0
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Country [68]
3566
0
Estonia
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State/province [68]
3566
0
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Country [69]
3567
0
Hong Kong
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State/province [69]
3567
0
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Country [70]
3568
0
Lithuania
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State/province [70]
3568
0
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Funding & Sponsors
Funding source category [1]
265000
0
Commercial sector/Industry
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Name [1]
265000
0
UCB Inc.
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Address [1]
265000
0
1950 Lake Park Drive, Smyrna GA 30080, USA
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Country [1]
265000
0
United States of America
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Primary sponsor type
Commercial sector/Industry
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Name
UCB Inc
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Address
1950 Lake Park Drive, Smyrna GA 30080, USA
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Country
United States of America
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Secondary sponsor category [1]
264091
0
None
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Name [1]
264091
0
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Address [1]
264091
0
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Country [1]
264091
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
266963
0
Leading Ethics Committee: CPP - Ile de France V1
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Ethics committee address [1]
266963
0
10, Pavilion Jacquard, 47, Bd De L'Hopital 75651 Paris Cedex 13
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Ethics committee country [1]
266963
0
France
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Date submitted for ethics approval [1]
266963
0
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Approval date [1]
266963
0
21/01/2011
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Ethics approval number [1]
266963
0
CPP no: 113-10
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Ethics committee name [2]
266964
0
Prof. Dr. J-M Maloteaux
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Ethics committee address [2]
266964
0
Avenue Hippocrate 53-14, Tour Harvey -Niveau 0, 1200 Bruxelles;
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Ethics committee country [2]
266964
0
Belgium
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Date submitted for ethics approval [2]
266964
0
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Approval date [2]
266964
0
21/02/2011
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Ethics approval number [2]
266964
0
OM 003
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Ethics committee name [3]
266965
0
Eticka Komise Revmatologickeho ustav
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Ethics committee address [3]
266965
0
Na Stupi4, 128-50 Praha 2
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Ethics committee country [3]
266965
0
Czech Republic
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Date submitted for ethics approval [3]
266965
0
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Approval date [3]
266965
0
21/12/2010
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Ethics approval number [3]
266965
0
6044/2010-
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Ethics committee name [4]
266966
0
National Institute of Pharmacy
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Ethics committee address [4]
266966
0
H-1051, Budapest, Zrinyi03 H-1372 Budapest, POB:450
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Ethics committee country [4]
266966
0
Hungary
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Date submitted for ethics approval [4]
266966
0
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Approval date [4]
266966
0
08/02/2011
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Ethics approval number [4]
266966
0
OGYI/54703-6/2010
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Ethics committee name [5]
266967
0
The Barzilai Medical Center
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Ethics committee address [5]
266967
0
Ben-Gurion University of the Negen
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Ethics committee country [5]
266967
0
Israel
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Date submitted for ethics approval [5]
266967
0
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Approval date [5]
266967
0
02/03/2011
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Ethics approval number [5]
266967
0
1703
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Ethics committee name [6]
266968
0
Helsinki Committee of Bnai Zion Medical Center
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Ethics committee address [6]
266968
0
Bnai Zion Medical Center, 43 Golomb St. , Haifa 31048,
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Ethics committee country [6]
266968
0
Israel
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Date submitted for ethics approval [6]
266968
0
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Approval date [6]
266968
0
21/01/2011
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Ethics approval number [6]
266968
0
0149-10-BNZ
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Ethics committee name [7]
266969
0
Pharma Ethics Ltd
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Ethics committee address [7]
266969
0
123 Amcor Road, Lyttelton Manor 0157
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Ethics committee country [7]
266969
0
South Africa
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Date submitted for ethics approval [7]
266969
0
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Approval date [7]
266969
0
07/03/2011
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Ethics approval number [7]
266969
0
11014093
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Ethics committee name [8]
266970
0
CEIC de Euskadi
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Ethics committee address [8]
266970
0
Comittico de Investigacin Clinica de la Comunidad Aut noma del Pas Vasco. CEIC-E, Direccin de Farmacia del Departamento de Sanidad, C/ Donostia - San Sebastin, 1, 01010 Vitoria - Alava
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Ethics committee country [8]
266970
0
Spain
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Date submitted for ethics approval [8]
266970
0
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Approval date [8]
266970
0
14/02/2011
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Ethics approval number [8]
266970
0
NAP
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Ethics committee name [9]
266971
0
Central Ethics Commission of Ministry of Health of Ukraine
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Ethics committee address [9]
266971
0
Vul. Narodnogo opolchennia, 5, Kyiv, 03680 MSP
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Ethics committee country [9]
266971
0
Ukraine
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Date submitted for ethics approval [9]
266971
0
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Approval date [9]
266971
0
16/03/2011
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Ethics approval number [9]
266971
0
#5.12-282/KE
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Ethics committee name [10]
266972
0
Ethics Committee Shalby Hospital
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Ethics committee address [10]
266972
0
Shalby Hospital, Opp. Karnavati Club, S.G. Road, Ahmedabad-380015,Gujarat
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Ethics committee country [10]
266972
0
India
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Date submitted for ethics approval [10]
266972
0
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Approval date [10]
266972
0
09/02/2011
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Ethics approval number [10]
266972
0
NAP
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Ethics committee name [11]
266973
0
Schulman Associates IRB, Inc.
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Ethics committee address [11]
266973
0
4290 Glendale-Milford Road Cincinnati, OH 45242
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Ethics committee country [11]
266973
0
United States of America
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Date submitted for ethics approval [11]
266973
0
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Approval date [11]
266973
0
10/12/2010
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Ethics approval number [11]
266973
0
201066940
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Summary
Brief summary
This is a Phase 3, multicenter, open-label, extension study to evaluate the safety, tolerability, efficacy, and immunogenicity of long-term epratuzumab treatment in subjects with SLE. Subjects who complete 1 of the Phase 3, double-blind, placebo controlled studies, SL0009 or SL0010, or terminate prematurely (at Week 16 or later) due to lack of efficacy, are eligible to enroll in SL0012. The study consists of an Open-Label Treatment Period and a Safety Follow-Up Visit. During the Open-Label Treatment Period, all subjects will receive epratuzumab 600mg delivered QW via slow iv infusion for a total of 4 consecutive weeks (CMD 2400mg) over eight 12 week treatment cycles (ie, Weeks 0, 1, 2, 3, 12, 13, 14, 15, 24, 25, 26, 27, 36, 37, 38, 39, 48 (Year 1), 49, 50, 51, 60, 61, 62, 63, 72, 73, 74, 75, 84, 85, 86, and 87 (Year 2) [96 weeks total duration]). A Safety Follow-Up Visit will occur approximately 4 weeks after Week 96 (ie, no later than Week 100) for subjects who complete the study, or 13 weeks after the final dose of study drug for subjects who discontinue early. Study drug treatment is in addition to the subjects’ existing standard care of oral corticosteroids and any immunosuppressants or antimalarials continued from Baseline in the subjects’ prior study.
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Trial website
www.embodyprogram.com
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
32561
0
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Address
32561
0
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Country
32561
0
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Phone
32561
0
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Fax
32561
0
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Email
32561
0
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Contact person for public queries
Name
15808
0
Dulce Lauterbach
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Address
15808
0
PAREXEL International Pty Ltd
Suite B Level 6, 15 Talavera Road
North Ryde NSW 2113
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Country
15808
0
Australia
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Phone
15808
0
+61 2 8870 3100 (reception) +61 2 8870 3191 (direct)
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Fax
15808
0
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Email
15808
0
[email protected]
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Contact person for scientific queries
Name
6736
0
Betsy Smith
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Address
6736
0
Clinical Project Manager
UCB BioSciences, Inc.
8010 Arco Corporate Drive, Suite 100
Raleigh, NC 27617
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Country
6736
0
United States of America
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Phone
6736
0
+1 919 767 2619
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Fax
6736
0
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Email
6736
0
[email protected]
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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
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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