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SE OF ABATACEPT IN ANCA-ASSOCIATED VASCULITIS - ABAVAS

Conditions
Patients with ANCA-associated Vasculitis
MedDRA version: 9.1Level: LLTClassification code 10047888Term: Wegener's granulomatosis
Registration Number
EUCTR2008-004138-26-IT
Lead Sponsor
AZIENDA OSPEDALIERA DI PARMA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
112
Inclusion Criteria

Males and females (not nursing and not pregnant) at least 18 years of age. Women of child bearing potential are eligible if they are practicing effective contraceptive measures With Acute AAV, presenting at first diagnosis or relapse (not grumblers, to maximize effect seen), defined by clinical presentation with Wegener?s Granulomatosis (WG), microscopic polyangiitis (MPA) or Churg-Strauss syndrome (CSS)* and ANCA positivity (anti-MPO or anti-PR3 positive) or historical ANCA positivity, and a BVAS score of > 8. Written informed consent given
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Those with severe life-threatening disease, i.e. lung haemorrhage at the time of presentation, renal impairment with SCr>150 mcmol/l, or severe CNS dysfunction thought to be due to vasculitis. Subjects with current symptoms of severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal, pulmonary, cardiac, neurological or cerebral disease, or other medical conditions that, in the opinion of the investigator, might place the subject at unacceptable risk for participation in this study. With any other non-vasculitic multisystem autoimmune disease. With any serious acute bacterial infection unless treated and completely resolved with antibiotics prior to enrollment With any severe chronic or recurrent bacterial infection, e g. bronchiectasis, osteomyelitis, chronic pyelonephritis With Hepatitis B or C or HIV. With Herpes zoster infection that resolved less than 2 months prior to enrollment. Subjects who have received any live vaccines* within 3 months of the first dose of study medication or who will have need of a live vaccine at any time in the year following enrollment.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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