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NCT05716334Completed

Biosimilars of Rituximab in ANCA-associated Vasculitis Compared to the Originator

Biosimilars of Rituximab in ANCA-associated Vasculitis Compared to the Originator (BRAVO): a CanVasc Multicentre Study

Source: ClinicalTrials.gov · Last updated 2 Dec 2025

Brief summary (registry, in English)

The goal of this multicentre observational study is to compare the safety and effectiveness of rituximab biosimilars to the originator in Canadian patients with Granulomatosis with Polyangiitis (GPA) and Microscopic Polyangiitis (MPA), two main forms of ANCA-associated vasculitis (AAV). The main questions it aims to answer are: * Is there a difference in vasculitis control between originator and biosimilar rituximab? * Is there a difference in adverse effects between originator and biosimilar rituximab? * In the Canadian healthcare context, are wait times to receive approval (financial coverage) for rituximab shorter for biosimilars compared to originators? Investigators will perform study assessments (including recording disease activity, damage, and adverse events) at the time of participants' usual clinical care visits, at regular intervals for 2 years after starting rituximab (for induction or maintenance treatment) or switching from an originator to a biosimilar as part of their usual care. Researchers will compare outcomes among participants who have received rituximab originators (from 2018 onwards) or biosimilars as part of their usual care, to see if there are differences in relapses, remission rates, damage, serious infections, serious adverse events, and treatment approval wait times.

Status (registry)
Completed
Study type
Observational
Enrollment
201 (actual)
First submitted
30 Nov 2022
Start date
15 Jun 2021
Primary completion date
15 Sept 2025
Lead sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre
NCT number
NCT05716334

What you commit to

  • Study type: Observational
  • Participants enrolled: 201
  • From 15 Jun 2021 to the primary completion date, 15 Sept 2025
  • 9 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • patients who did not/are not receiving RTX induction or maintenance therapy
  • patients who initiated most recent RTX treatment course prior to Jan 1, 2018
  • patients receiving RTX for reasons other than GPA or MPA induction or maintenance (e.g. other concurrent disease)

Other

  • patients without a diagnosis of GPA or MPA
  • unable to provide informed consent

Who the study is looking for

  • Prospective cohort:
  • Initiated within the last 6 months:
  • RTX biosimilar or originator for induction OR
  • RTX biosimilar or originator for maintenance (with or without prior RTX induction) OR
  • Switched from RTX originator maintenance to biosimilar maintenance (4-12 months between infusions)
    • Historical cohort:
    • Followed in a prospective longitudinal cohort study/registry within the CanVasc network, and initiated the following after January 1, 2018 but \>6 months prior to study enrollment
  • RTX biosimilar or originator for induction OR
  • RTX biosimilar or originator for maintenance (with or without RTX induction)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Of Calgary
Coordinator of this site? Confirm its status
CalgaryCanadaUnknown status
University of Alberta
Coordinator of this site? Confirm its status
EdmontonCanadaUnknown status
St Joseph's Healthcare Hamilton (McMaster University)
Coordinator of this site? Confirm its status
HamiltonCanadaUnknown status
Lawson Research Institute (Western University)
Coordinator of this site? Confirm its status
LondonCanadaUnknown status
McGill University (Montreal General Hospital)
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status
Centre Intégré Universitaire de Santé et de Services Sociaux du Nord-de-l'île-de-Montréal (CIUSSS NÎM) / Hôpital du Sacré-Coeur de Montréal
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status
Ottawa Hospital Research Institute (Ottawa University)
Coordinator of this site? Confirm its status
OttawaCanadaUnknown status
Sinai Health System (University of Toronto)
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
University of British Columbia (Vancouver Coastal Health Authority)
Coordinator of this site? Confirm its status
VancouverCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.