Belimumab in Remission of VASculitis
Sponsored by Human Genome Sciences Inc., a GSK Company
About this trial
Last updated 7 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Ended 8 years ago
What is this trial about?
What are the Participation Requirements?
Key Inclusion Criteria:
- Clinical diagnosis Wegener's granulomatosis or microscopic polyangiitis by Chapel
Hill criteria.
- Disease flare in the past 26 weeks requiring treatment with high dose
corticosteroids and 1 of the following medications: rituximab, oral cyclophosphamide
OR IV cyclophosphamide.
- Tested positive for anti-proteinase 3 (anti-PR3) or anti-myeloperoxidase (anti-MPO)
antibodies at any time prior to enrollment.
- Achieve remission no more than 26 weeks after first dose of induction treatment.
Remission is defined as a Birmingham Vasculitis Activity (BVAS) score of 0 and
receiving less than 10 mg/day of oral prednisone (or equivalent) on 2 consecutive
visits 21 to 35 days apart.
- Maintenance therapy on this study must start no more than 2 weeks after confirmation
of remission.
Key Exclusion Criteria:
- Pregnant or nursing.
- Receipt of a B cell targeted therapy (other than rituximab) at anytime
- Receipt of an investigational biological agent within the past 60 days.
- Required management of acute or chronic infections within the past 60 days.
- Current drug or alcohol abuse or dependence.
- Current or past positive test for human immunodeficiency virus (HIV), hepatitis B,
or hepatitis C.
- History of severe allergic reaction to contrast agents or biological medicines.