BIANCA-SC: A Study of the Efficacy, Safety, and Tolerability of Blisibimod in Addition to Methotrexate During Induction of Remission in Subjects With ANCA-Associated Small Vessel Vasculitis (BIANCA-SC)
Primary Purpose
Granulomatosis With Polyangiitis, Microscopic Polyangiitis
Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Blisibimod
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Granulomatosis With Polyangiitis focused on measuring granulomatosis with polyangiitis, microscopic polyangiitis, anti-neutrophil cytoplasmic antibodies, ANCA-associated vasculitis, Wegener Granulomatosis
Eligibility Criteria
Inclusion Criteria:
- 18 years of age or older (male or female).
- Granulomatosis with polyangiitis (GPA, or Wegener's granulomatosis) or microscopic polyangiitis (MPA) according to the definitions of the American College of Rheumatology and Chapel Hill Consensus Conference.
- Active GPA or MPA disease at screening.
- Positive for either PR3-ANCA or MPO-ANCA at screening.
- Subject willing to initiate corticosteroids and methotrexate (MTX) if not already on corticosteroids and/or MTX at baseline.
- Clinical intention to prescribe MTX therapy for treatment of GPA or MPA.
Exclusion Criteria:
- Diagnosed with Churg Strauss syndrome.
- Severe GPA or MPA disease that would conventionally be treated with cyclophosphamide.
- Nursing or pregnant.
- Active systemic infection or deep-space infection.
- Active hepatitis B, active hepatitis C or a documented history of HIV, hepatitis B, or hepatitis C.
- Liver disease.
- History of documented anti-glomerular basement membrane (GBM) disease.
- Malignancy within the past 5 years.
- History of active tuberculosis (TB) or history of TB infection.
- Anemia, neutropenia, or thrombocytopenia.
- Serum creatinine level greater than 2.5 mg/dL.
- Prior administration of a B-cell modulating therapy other than rituximab.
- Subject has not yet completed at least 3 months or 5 half-lives (whichever is longer) since ending other investigational study.
- History of congenital immunodeficiency.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Blisibimod
Placebo
Arm Description
Outcomes
Primary Outcome Measures
Induction of clinical remission
Clinical remission includes the ability to taper corticosteroids.
Secondary Outcome Measures
Time to complete remission
Time to treatment failure
Ability to taper corticosteroids
Change in baseline BVAS/WG score
Safety profile
Compare biomarker changes from baseline
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01598857
Brief Title
BIANCA-SC: A Study of the Efficacy, Safety, and Tolerability of Blisibimod in Addition to Methotrexate During Induction of Remission in Subjects With ANCA-Associated Small Vessel Vasculitis
Acronym
BIANCA-SC
Official Title
A Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of Blisibimod in Addition to Methotrexate During Induction of Remission in Subjects With ANCA-Associated Small Vessel Vasculitis
Study Type
Interventional
2. Study Status
Record Verification Date
July 2015
Overall Recruitment Status
Withdrawn
Study Start Date
December 2014 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Anthera Pharmaceuticals
4. Oversight
5. Study Description
Brief Summary
The purpose of this study is to evaluate efficacy, safety and tolerability of blisibimod when taken with methotrexate in the induction of remission in ANCA-Associated Small Vessel Vasculitis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Granulomatosis With Polyangiitis, Microscopic Polyangiitis
Keywords
granulomatosis with polyangiitis, microscopic polyangiitis, anti-neutrophil cytoplasmic antibodies, ANCA-associated vasculitis, Wegener Granulomatosis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Blisibimod
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Blisibimod
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Induction of clinical remission
Description
Clinical remission includes the ability to taper corticosteroids.
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Time to complete remission
Time Frame
Various timepoints to 24 weeks
Title
Time to treatment failure
Time Frame
Various timepoints to 24 weeks
Title
Ability to taper corticosteroids
Time Frame
Various timepoints to 24 weeks
Title
Change in baseline BVAS/WG score
Time Frame
Various timepoints to 24 weeks
Title
Safety profile
Time Frame
Various timepoints to 24 weeks
Title
Compare biomarker changes from baseline
Time Frame
Various timepoints to 24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years of age or older (male or female).
Granulomatosis with polyangiitis (GPA, or Wegener's granulomatosis) or microscopic polyangiitis (MPA) according to the definitions of the American College of Rheumatology and Chapel Hill Consensus Conference.
Active GPA or MPA disease at screening.
Positive for either PR3-ANCA or MPO-ANCA at screening.
Subject willing to initiate corticosteroids and methotrexate (MTX) if not already on corticosteroids and/or MTX at baseline.
Clinical intention to prescribe MTX therapy for treatment of GPA or MPA.
Exclusion Criteria:
Diagnosed with Churg Strauss syndrome.
Severe GPA or MPA disease that would conventionally be treated with cyclophosphamide.
Nursing or pregnant.
Active systemic infection or deep-space infection.
Active hepatitis B, active hepatitis C or a documented history of HIV, hepatitis B, or hepatitis C.
Liver disease.
History of documented anti-glomerular basement membrane (GBM) disease.
Malignancy within the past 5 years.
History of active tuberculosis (TB) or history of TB infection.
Anemia, neutropenia, or thrombocytopenia.
Serum creatinine level greater than 2.5 mg/dL.
Prior administration of a B-cell modulating therapy other than rituximab.
Subject has not yet completed at least 3 months or 5 half-lives (whichever is longer) since ending other investigational study.
History of congenital immunodeficiency.
12. IPD Sharing Statement
Learn more about this trial
BIANCA-SC: A Study of the Efficacy, Safety, and Tolerability of Blisibimod in Addition to Methotrexate During Induction of Remission in Subjects With ANCA-Associated Small Vessel Vasculitis
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