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Phase 3 N=170 Randomized Treatment

Rituximab Vasculitis Maintenance Study

Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis · Microscopic Polyangiitis · Wegener Granulomatosis

Enrolled (actual)
170
Serious AEs
29.4%
Results posted
Mar 2022
Primary outcome: Primary: Relapse-free Survival — 38; 60; 13; 32 participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Rituximab (Biological); Azathioprine (Drug)
Age
Pediatric, Adult, Older Adult · 15+ yrs
Sex
All
Sponsor
Cambridge University Hospitals NHS Foundation Trust
Primary completion
Nov 2018

Outcome Measures

OutcomeResultp-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
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
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
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
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

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.

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01697267). 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.

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