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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Withdrawn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
Anthera Pharmaceuticals
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 18 years of age or older (male or female).
  2. 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.
  3. Active GPA or MPA disease at screening.
  4. Positive for either PR3-ANCA or MPO-ANCA at screening.
  5. Subject willing to initiate corticosteroids and methotrexate (MTX) if not already on corticosteroids and/or MTX at baseline.
  6. Clinical intention to prescribe MTX therapy for treatment of GPA or MPA.

Exclusion Criteria:

  1. Diagnosed with Churg Strauss syndrome.
  2. Severe GPA or MPA disease that would conventionally be treated with cyclophosphamide.
  3. Nursing or pregnant.
  4. Active systemic infection or deep-space infection.
  5. Active hepatitis B, active hepatitis C or a documented history of HIV, hepatitis B, or hepatitis C.
  6. Liver disease.
  7. History of documented anti-glomerular basement membrane (GBM) disease.
  8. Malignancy within the past 5 years.
  9. History of active tuberculosis (TB) or history of TB infection.
  10. Anemia, neutropenia, or thrombocytopenia.
  11. Serum creatinine level greater than 2.5 mg/dL.
  12. Prior administration of a B-cell modulating therapy other than rituximab.
  13. Subject has not yet completed at least 3 months or 5 half-lives (whichever is longer) since ending other investigational study.
  14. 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

    First Posted
    May 11, 2012
    Last Updated
    July 28, 2015
    Sponsor
    Anthera Pharmaceuticals
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    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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