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
This study is not yet open for participant recruitment.
Verified March 2013 by Anthera Pharmaceuticals
Sponsor:
Anthera Pharmaceuticals
Information provided by (Responsible Party):
Anthera Pharmaceuticals
ClinicalTrials.gov Identifier:
NCT01598857
First received: May 11, 2012
Last updated: March 20, 2013
Last verified: March 2013
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Granulomatosis With Polyangiitis Microscopic Polyangiitis |
Drug: Blisibimod Drug: Placebo |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| 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 |
Resource links provided by NLM:
Further study details as provided by Anthera Pharmaceuticals:
Primary Outcome Measures:
- Induction of clinical remission [ Time Frame: 24 weeks ] [ Designated as safety issue: No ]Clinical remission includes the ability to taper corticosteroids.
Secondary Outcome Measures:
- Time to complete remission [ Time Frame: Various timepoints to 24 weeks ] [ Designated as safety issue: No ]
- Time to treatment failure [ Time Frame: Various timepoints to 24 weeks ] [ Designated as safety issue: No ]
- Ability to taper corticosteroids [ Time Frame: Various timepoints to 24 weeks ] [ Designated as safety issue: No ]
- Change in baseline BVAS/WG score [ Time Frame: Various timepoints to 24 weeks ] [ Designated as safety issue: No ]
- Safety profile [ Time Frame: Various timepoints to 24 weeks ] [ Designated as safety issue: Yes ]
- Compare biomarker changes from baseline [ Time Frame: Various timepoints to 24 weeks ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 100 |
| Study Start Date: | December 2013 |
| Estimated Primary Completion Date: | June 2015 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Blisibimod | Drug: Blisibimod |
| Placebo Comparator: Placebo | Drug: Placebo |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
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.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01598857
Contacts
| Contact: Colin Hislop | chislop@anthera.com |
Sponsors and Collaborators
Anthera Pharmaceuticals
More Information
No publications provided
| Responsible Party: | Anthera Pharmaceuticals |
| ClinicalTrials.gov Identifier: | NCT01598857 History of Changes |
| Other Study ID Numbers: | AN-VAS3321 |
| Study First Received: | May 11, 2012 |
| Last Updated: | March 20, 2013 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Anthera Pharmaceuticals:
|
granulomatosis with polyangiitis microscopic polyangiitis anti-neutrophil cytoplasmic antibodies ANCA-associated vasculitis Wegener Granulomatosis |
Additional relevant MeSH terms:
|
Vasculitis Systemic Vasculitis Microscopic Polyangiitis Vascular Diseases Cardiovascular Diseases Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Autoimmune Diseases Immune System Diseases Methotrexate Antibodies, Antineutrophil Cytoplasmic Abortifacient Agents, Nonsteroidal Abortifacient Agents Reproductive Control Agents Physiological Effects of Drugs |
Pharmacologic Actions Therapeutic Uses Antimetabolites, Antineoplastic Antimetabolites Molecular Mechanisms of Pharmacological Action Antineoplastic Agents Dermatologic Agents Enzyme Inhibitors Folic Acid Antagonists Immunosuppressive Agents Immunologic Factors Antirheumatic Agents Nucleic Acid Synthesis Inhibitors |
ClinicalTrials.gov processed this record on May 19, 2013