A Study to Evaluate Two Doses of Ocrelizumab in Patients With Active Systemic Lupus Erythematosus (BEGIN) (BEGIN)
Primary Purpose
Systemic Lupus Erythematosus
Status
Terminated
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Prednisone
Immunosuppressive regime (azathioprine, mycophenolate mofetil or methotrexate)
Methylprednisolone
Ocrelizumab
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Systemic Lupus Erythematosus focused on measuring SLE
Eligibility Criteria
Inclusion Criteria:
- Age 16 years or above at the time of screening
- Diagnosis of SLE
- Active disease at screening
Exclusion Criteria:
- Presence of active moderate to severe glomerulonephritis
- Currently active retinitis, poorly controlled seizure disorder, acute confusional state, myelitis, stroke or stroke syndrome, cerebellar ataxia, or dementia
- Lack of peripheral venous access
- Pregnancy or breast feeding mothers
- History of severe allergic or anaphylactic reactions to humanized, chimeric or murine monoclonal antibodies or i.v. immunoglobulin
- Known severe chronic pulmonary disease
- Evidence of significant or uncontrolled concomitant diseases in any organ system not related to SLE, which, in the investigator's opinion, would impair patient participation
- Concomitant condition which has required treatment with systemic corticosteroid (excluding topical or inhaled) at any time in the 52 weeks prior to screening
- Known HIV or chronic active Hepatitis B or chronic active Hepatitis C infection
- Known active infection of any kind (but excluding fungal infection of nail beds or oral thrush which has resolved before Day 1) within 30 days prior to Day 1. In addition, any major episode of infection requiring hospitalization or treatment with intravenous anti-infectives in the 30 days prior to Day 1 or oral anti-infectives in the 14 days prior to Day 1
- History of serious recurrent or chronic infection
- History of cancer (except basal cell carcinoma of the skin that has been excised and cured)
- History of alcohol or drug abuse in the 52 weeks prior to screening
- Major surgery in the 4 weeks prior to screening excluding diagnostic surgery
- Previous treatment with CAMPATH-1H
- Previous treatment with a BAFF directed treatment in the 12 months prior to screening
- Previous treatment with a B-cell targeted therapy other than one directed at BAFF
- Treatment with any investigational agent, other than those above, in the 28 days prior to screening or five half-lives of the investigational drug (whichever is longer)
- Receipt of any live vaccine in the 6 weeks prior to Day 1
- Intolerance or contraindication to oral or i.v. corticosteroids
- Treatment with a second immunosuppressive or immunomodulatory drug in the 8 weeks prior to Day 1
- Prednisone dose of ≥ 0.7 mg/kg/day (or equivalent) for > 7 of the previous 30 days prior to screening
- Treatment with cyclophosphamide or a calcineurin inhibitor in the 12 weeks prior to screening
- Positive hepatitis BsAg or hepatitis C serology. Patients who are HBsAg negative but HBcAb positive may be enrolled with a negative DNA test
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Ocrelizumab 1000 mg
Ocrelizumab 400 mg
Placebo
Arm Description
Ocrelizumab was administered i.v. at a dose on Days 1 and 15, followed by 1000 mg i.v. at Week 16 and then every 16 weeks
Ocrelizumab was administered at a dose 400 mg i.v. on Days 1 and 15, followed by 400 mg i.v. at Week 16 and then every 16 weeks
Placebo infusions were administered on Days 1 and 15, followed by placebo infusion at Week 16 and then every 16 weeks
Outcomes
Primary Outcome Measures
Number of Participants With Major Clinical Response (MCR)
Number of Participants With Partial Clinical Response (PCR)
Number of Non-responders (NR)
Secondary Outcome Measures
Number of Participants Who Achieved a BILAG Score of C or Better at Week 24.
Time Adjusted Mean SLEDAI-2K Score
Annualized Flare Rate
Time to First Moderate to Severe Flare
Number of Participants Who Achieved A Major Or Partial Clinical Response At Week 48 (PCR Plus MCR Proportion), Who Did Not Experience A Flare Before Week 96
Number of Participants Who Achieved A MCR At Week 48, Who Did Not Experience A Flare Before Week 72
Number of Participants Achieved A MCR At Week 48, Who Did Not Experience A Flare Before Week 96
Change in SF-36 Subscale And Summary Scores From Baseline At Week 48
Change In FACIT-Fatigue Assessment From Baseline To Week 48
Change From Baseline In Pain Quality And Impact Of Pain On Daily Function Measured By The Brief Pain Inventory Short Form At Week 48
The EQ-5D Single Index Utility Score At Week 48
Number of Participants With Adverse Events
Full Information
NCT ID
NCT00539838
First Posted
October 3, 2007
Last Updated
August 27, 2020
Sponsor
Genentech, Inc.
Collaborators
Roche Pharma AG
1. Study Identification
Unique Protocol Identification Number
NCT00539838
Brief Title
A Study to Evaluate Two Doses of Ocrelizumab in Patients With Active Systemic Lupus Erythematosus (BEGIN)
Acronym
BEGIN
Official Title
A Randomised, Double-Blind, Placebo Controlled, Parallel-Group, Multicenter Study to Evaluate the Efficacy and Safety of Two Doses of Ocrelizumab in Patients With Active Systemic Lupus Erythematosus
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Terminated
Why Stopped
The study was terminated prematurely when the decision was made that ocrelizumab was not likely to benefit this patient population.
Study Start Date
December 19, 2007 (Actual)
Primary Completion Date
July 12, 2011 (Actual)
Study Completion Date
July 12, 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Genentech, Inc.
Collaborators
Roche Pharma AG
4. Oversight
5. Study Description
Brief Summary
This is a Phase III, randomized, double blind, placebo-controlled, multicenter, parallel-group study to evaluate the efficacy and safety of ocrelizumab compared to placebo when combined with a single stable background immunosuppressive medication and a corticosteroid regimen in patients with moderately to severely active systemic lupus erythematosus, who do not have moderate to severe glomerulonephritis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Systemic Lupus Erythematosus
Keywords
SLE
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
33 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ocrelizumab 1000 mg
Arm Type
Experimental
Arm Description
Ocrelizumab was administered i.v. at a dose on Days 1 and 15, followed by 1000 mg i.v. at Week 16 and then every 16 weeks
Arm Title
Ocrelizumab 400 mg
Arm Type
Experimental
Arm Description
Ocrelizumab was administered at a dose 400 mg i.v. on Days 1 and 15, followed by 400 mg i.v. at Week 16 and then every 16 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo infusions were administered on Days 1 and 15, followed by placebo infusion at Week 16 and then every 16 weeks
Intervention Type
Drug
Intervention Name(s)
Prednisone
Intervention Description
Oral repeating dose
Intervention Type
Drug
Intervention Name(s)
Immunosuppressive regime (azathioprine, mycophenolate mofetil or methotrexate)
Intervention Description
Oral repeating dose
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone
Intervention Description
Intravenous repeating dose
Intervention Type
Drug
Intervention Name(s)
Ocrelizumab
Intervention Description
Intravenous repeating dose
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Intravenous repeating dose
Primary Outcome Measure Information:
Title
Number of Participants With Major Clinical Response (MCR)
Time Frame
Week 48
Title
Number of Participants With Partial Clinical Response (PCR)
Time Frame
Week 48
Title
Number of Non-responders (NR)
Time Frame
Week 48
Secondary Outcome Measure Information:
Title
Number of Participants Who Achieved a BILAG Score of C or Better at Week 24.
Time Frame
Week 24
Title
Time Adjusted Mean SLEDAI-2K Score
Time Frame
Week 48
Title
Annualized Flare Rate
Time Frame
Week 48 to Week 96
Title
Time to First Moderate to Severe Flare
Time Frame
Week 48 to Week 96
Title
Number of Participants Who Achieved A Major Or Partial Clinical Response At Week 48 (PCR Plus MCR Proportion), Who Did Not Experience A Flare Before Week 96
Time Frame
Week 48 to Week 96
Title
Number of Participants Who Achieved A MCR At Week 48, Who Did Not Experience A Flare Before Week 72
Time Frame
Week 48 to Week 72
Title
Number of Participants Achieved A MCR At Week 48, Who Did Not Experience A Flare Before Week 96
Time Frame
Week 48 to Week 96
Title
Change in SF-36 Subscale And Summary Scores From Baseline At Week 48
Time Frame
Baseline, Week 48
Title
Change In FACIT-Fatigue Assessment From Baseline To Week 48
Time Frame
Baseline, Week 48
Title
Change From Baseline In Pain Quality And Impact Of Pain On Daily Function Measured By The Brief Pain Inventory Short Form At Week 48
Time Frame
Baseline, Week 48
Title
The EQ-5D Single Index Utility Score At Week 48
Time Frame
Baseline, Week 48
Title
Number of Participants With Adverse Events
Time Frame
Up to 2.5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 16 years or above at the time of screening
Diagnosis of SLE
Active disease at screening
Exclusion Criteria:
Presence of active moderate to severe glomerulonephritis
Currently active retinitis, poorly controlled seizure disorder, acute confusional state, myelitis, stroke or stroke syndrome, cerebellar ataxia, or dementia
Lack of peripheral venous access
Pregnancy or breast feeding mothers
History of severe allergic or anaphylactic reactions to humanized, chimeric or murine monoclonal antibodies or i.v. immunoglobulin
Known severe chronic pulmonary disease
Evidence of significant or uncontrolled concomitant diseases in any organ system not related to SLE, which, in the investigator's opinion, would impair patient participation
Concomitant condition which has required treatment with systemic corticosteroid (excluding topical or inhaled) at any time in the 52 weeks prior to screening
Known HIV or chronic active Hepatitis B or chronic active Hepatitis C infection
Known active infection of any kind (but excluding fungal infection of nail beds or oral thrush which has resolved before Day 1) within 30 days prior to Day 1. In addition, any major episode of infection requiring hospitalization or treatment with intravenous anti-infectives in the 30 days prior to Day 1 or oral anti-infectives in the 14 days prior to Day 1
History of serious recurrent or chronic infection
History of cancer (except basal cell carcinoma of the skin that has been excised and cured)
History of alcohol or drug abuse in the 52 weeks prior to screening
Major surgery in the 4 weeks prior to screening excluding diagnostic surgery
Previous treatment with CAMPATH-1H
Previous treatment with a BAFF directed treatment in the 12 months prior to screening
Previous treatment with a B-cell targeted therapy other than one directed at BAFF
Treatment with any investigational agent, other than those above, in the 28 days prior to screening or five half-lives of the investigational drug (whichever is longer)
Receipt of any live vaccine in the 6 weeks prior to Day 1
Intolerance or contraindication to oral or i.v. corticosteroids
Treatment with a second immunosuppressive or immunomodulatory drug in the 8 weeks prior to Day 1
Prednisone dose of ≥ 0.7 mg/kg/day (or equivalent) for > 7 of the previous 30 days prior to screening
Treatment with cyclophosphamide or a calcineurin inhibitor in the 12 weeks prior to screening
Positive hepatitis BsAg or hepatitis C serology. Patients who are HBsAg negative but HBcAb positive may be enrolled with a negative DNA test
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jorn Drappa, M.D., Ph.D.
Organizational Affiliation
Genentech, Inc.
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Qualified researchers may request access to individual patient level data through the clinical study data request platform (www.vivli.org). Further details on Roche's criteria for eligible studies are available here (https://vivli.org/members/ourmembers/). For further details on Roche's Global Policy on the Sharing of Clinical Information and how to request access to related clinical study documents, see here (https://www.roche.com/research_and_development/who_we_are_how_we_work/clinical_trials/our_commitment_to_data_sharing.htm).
Links:
URL
http://www.roche-trials.com/trialDetailsGet.action?studyNumber=WA20499&productGenericName=ocrelizumab&productType=Drug&divisionName=PHA
Description
Ex-U.S. Study Information (Ex-US this trial is sponsored/managed by Hoffmann-La Roche)
Learn more about this trial
A Study to Evaluate Two Doses of Ocrelizumab in Patients With Active Systemic Lupus Erythematosus (BEGIN)
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