Phase 3
Completed N=170
Rituximab Vasculitis Maintenance Study
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis · Microscopic Polyangiitis · Wegener Granulomatosis
Source: ClinicalTrials.gov NCT01697267 ↗
Enrolled (actual)
170
Serious AEs
29.4%
Results posted
Mar 2022
Primary outcomePrimary: Relapse-free Survival — 38; 60; 13; 32 participants
◆ Published Evidence
Highly cited
119citations · ~40 / year
Rituximab versus azathioprine for maintenance of remission for patients with ANCA-associated vasculitis and relapsing disease: an international randomised controlled trial.
Summary
Rituximab is now established as an effective drug for anti-neutrophil cytoplasmic antibody (ANCA) vasculitis following major European and US trials reported in 2010. After a time, its effect wears off and the disease can return. This occurs in at least half of patients within 2 years of receiving Rituximab. A preliminary study in Cambridge has suggested that repeating rituximab every six months stops the disease returning and is safe.
The RITAZAREM trial will find out whether repeating rituximab stops vasculitis returning and whether it works better than the older treatments, azathioprine or methotrexate. It will also tell us how long patients remain well after the repeated rituximab treatments are stopped, and if repeated rituximab is safe. We should also learn useful information about the effects of rituximab on quality of life and economic measures. The trial results will help decide the best treatment for future patients who have their vasculitis initially treated with rituximab.
RITAZAREM aims to recruit patients with established ANCA vasculitis whose disease has come back 'relapsing vasculitis'. All patients will be treated with rituximab and steroids and we anticipate that most will respond well. If their disease is under reasonable control after four months, further treatment with either rituximab (a single dose ever four months for two years) or azathioprine tablets will be chosen randomly. The patients in the rituximab and azathioprine groups will then be compared. Patients will be in the trial for four years.
The study has been designed by members of the European Vasculitis Study group (EUVAS) and the Vasculitis Clinical Research Consortium (VCRC). It will include 190 participants from 30 hospitals in Europe, the USA, Australia and Mexico.
RITAZAREM is being funded by Arthritis Research UK, the U.S. National Institutes of Health and by Roche/Genentech.
Linked Publications (2)
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Rituximab versus azathioprine for maintenance of remission for patients with ANCA-associated vasculitis and relapsing disease: an international randomised controlled trial.
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Rituximab versus azathioprine as therapy for maintenance of remission for anti-neutrophil cytoplasm antibody-associated vasculitis (RITAZAREM): study protocol for a randomized controlled trial.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Relapse-free Survival |
38; 60; 13; 32; 25; 28 | — |
| SECONDARY Number of Participants in Remission at 24 and 48 Months |
73; 70; 54; 44 | — |
| SECONDARY Combined Damage Assessment Score (Disease Related Damage Assessment) |
0.275; 0.337; 0.571; 0.533; 0.676; 0.899 | — |
| SECONDARY Cumulative GC Exposure |
3717; 4780; 2184; 2426 | — |
| SECONDARY Severe Adverse Event Rate |
37; 48 | — |
| SECONDARY Infection Rates |
54; 62 | — |
| SECONDARY Health-related Quality of Life Using the SF-36 Physical Composite |
35.8; 35.0 | — |
| SECONDARY Health-related Quality of Life Using the SF-36 Mental Composite |
50.9; 53.9 | — |
Eligibility Criteria
Inclusion Criteria
- A diagnosis of AAV [granulomatosis with polyangiitis or microscopic polyangiitis], according to the definitions of the Chapel Hill Consensus Conference
- Current or historical PR3/MPO ANCA positivity by ELISA
- Disease relapse defined by one major or three minor disease activity items on the Birmingham Vasculitis Activity Score for Wegeners (BVAS/WG), in patients that have previously achieved remission following at least 3 months of induction therapy, with a combination of glucocorticoids and an immunosuppressive agent (cyclophosphamide or methotrexate or rituximab or mycophenolate mofetil)
- Written informed consent
Exclusion Criteria
- Age 2.5 times the upper limit of normal, unless attributed to vasculitis
Data sourced from ClinicalTrials.gov (NCT01697267) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.