Alemtuzumab for ANCA Associated Refractory Vasculitis - a Study of Safety and Efficacy
Alemtuzumab for ANCA Associated Refractory Vasculitis - a Study of Safety and Efficacy
Overview:
This open label, randomized, multi-centre study will enroll and treat 24 patients with refractory AAV.
Aims:
To determine the clinical response and severe adverse event rates associated with alemtuzumab therapy among patients with relapsing or refractory ANCA associated vasculitis (AAV).
Hypothesis:
Treatment with alemtuzumab induces sustained remission in AAV and will reduce immunosuppressive and steroid exposure.
Inclusion Criteria:
Exclusion Criteria:
Age less than 18 or greater than 60 years
Creatinine > 150μmol/l (1.7mg/dl)
Total white count < 4x109/l or lymphocyte count < 0.5x109/l, or IgG < 5g/L, or neutrophil count < 1.5x109/l.
Severe lung haemorrhage with hypoxia (<85% on room air)
Severe gastrointestinal, central nervous system or cardiac vasculitis
Previous therapy with:
Intensive care unit requirement
Active infection with HIV, hepatitis B or hepatitis C or other infection requiring parenteral or long-term oral antibiotics
History of ITP or platelet count at screening below 50,000 x 106/l
Pregnancy or inadequate contraception in pre-menopausal women
Breast feeding
Any condition judged by the investigator that would cause the study to be detrimental to the patient.
Any other multisystem autoimmune disease including Churg Strauss angiitis, systemic lupus erythematosus, anti-GBM disease and cryoglobulinaemia
Any previous or current history of malignancy (other than resected basal cell carcinoma)
dj106@cam.ac.uk00441223586796
ronasmith@doctors.net.uk00441223217259