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Observing Real-World Use of Avacopan in ANCA-Associated Vasculitis

Observes how avacopan is used in people with ANCA-associated vasculitis across Europe.

Plain-language title generated from the registry record
Registry title: Early-access Avacopan in Real-world ANCA-associated Vasculitis

Key facts

Where
Leiden, NetherlandsSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for people with GPA or MPA (types of ANCA-associated vasculitis) who start treatment with avacopan.

Age
16 years and older
Sex
All sexes
Disease stage
Established diagnosis of GPA or MPA, with disease activity that can be shown by a clinical measure or assessment.
Earlier treatment
Starting treatment with avacopan.

Main reasons for not taking part

  • No disease activity that can be shown by a clinical measure or assessment
  • Younger than 16 years

Read by machine on 12 November 2026.

Where in Netherlands

  • Leiden University Medical CenterLeiden, NetherlandsContact: YKO Teng, MD, PhDTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Leiden University Medical Center
Trial code
NCT06794827
Record updated
27 January 2025
Original description
The current study proposal aims to investigate the clinical practice variation of the initial use of avacopan for AAV patients in Europe. The study will describe patient characteristics and organ-specific clinical benefit of avacopan treatment in a unique, first-experience cohort of AAV patients. By studying the clinical practice variation of first-experience avacopan treatment, this study will be uniquely positioned to identify pivotal issues on the real-life implementation of avacopan treatment. These observational data can ultimately serve to address current knowledge gaps on avacopan treatment in AAV patients, improve the care and drug-access for AAV patients with avacopan treatment and generate new areas of research.Read full original descriptionShow less

Evaluating Clinical Practice of Early Access Avacopan Treatment for ANCA-associated Vasculitis in European Countries

The current study proposal aims to investigate the clinical practice variation of the initial use of avacopan for AAV patients in Europe. The study will describe patient characteristics and organ-specific clinical benefit of avacopan treatment in a unique, first-experience cohort of AAV patients. By studying the clinical practice variation of first-experience avacopan treatment, this study will be uniquely positioned to identify pivotal issues on the real-life implementation of avacopan treatment. These observational data can ultimately serve to address current knowledge gaps on avacopan treatment in AAV patients, improve the care and drug-access for AAV patients with avacopan treatment and generate new areas of research.

Inclusion: Established diagnosis of GPA or MPA; Treatment (initiation) with avacopan; Informed consent for use of medical data.

Exclusion: If there is no AAV disease activity present that can be supported by an objectifiable clinical measure or assessment; If a subject is below 16 years old.

ClinicalTrials.gov NCT06794827