This website uses cookies to enhance your browsing experience, improve site performance, and gather analytics. By selecting 'Accept,' you consent to these cookies as described in our Privacy Policy.

Belimumab in Remission of VASculitis

Sponsored by Human Genome Sciences Inc., a GSK Company

About this trial

Last updated 7 years ago

Study ID

115466

Status

Completed

Type

Interventional

Phase

Phase 3

Placebo

Yes

Accepting

18-75 Years
18+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 8 years ago

What is this trial about?

The purpose of this study is to evaluate the efficacy and safety of belimumab, in combination with azathioprine, for the maintenance of remission following a standard induction regimen in patients with Wegener's granulomatosis or microscopic polyangiitis. The random assignment in this study is "1 to 1" which means that participants have an equal chance of receiving belimumab or placebo.

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.

Locations

Location

Status