Vasculitis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with a condition called MPA (microscopic polyangiitis) or GPA (granulomatosis with polyangiitis), regardless of their ANCA blood test result
- People aged 18 years or older
- People whose condition is either newly diagnosed or has come back after a period of remission, and whose disease is currently inactive (confirmed by a disease activity score of zero)
- People who are currently receiving maintenance doses of a medication called rituximab, given at 6 months and 12 months after their initial treatment began
- People who are taking between 5 and 10 mg per day of prednisone (a steroid) at the time of the screening visit, and exactly 5 mg per day at the time of the enrolment visit
- People who are able to provide written consent to take part in the study before it begins
Who may not be able to join:
- People who have a different type of vasculitis (blood vessel inflammation), such as EGPA or others classified under recognised medical classification systems
- People whose vasculitis is currently active (confirmed by a disease activity score above zero)
- People who have an active infection, either current or ongoing, including HIV, hepatitis B, or hepatitis C
- People who currently have cancer, or who have had cancer within the past 5 years — though certain low-risk skin cancers and prostate cancer well-controlled by hormone treatment may be considered (confirm with trial site)
- People who are pregnant or breastfeeding; people who could become pregnant would need to use reliable contraception for the entire duration of the study
- People who have other serious uncontrolled health conditions — including severe mental health conditions or drug or alcohol dependency — that could affect their ability to participate
- People who have taken part in another clinical drug trial within the previous 3 months
- People who are considered unlikely to follow the treatment plan as required by the study
- People whose white blood cell count is at or below 4,000 per mm³
- People whose platelet count is at or below 100,000 per mm³
- People whose liver enzyme levels (ALT or AST) are more than 3 times the accepted normal upper limit, where this cannot be explained by their MPA or GPA condition
- People who are unable to provide written consent to participate
- People for whom rituximab is medically unsuitable or contraindicated
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Jean-Christophe LEGA, Pr, Hospices Civils de Lyon
Phone: 04.78.86.19.79
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Relapse-free survival, relapse being defined as BVAS > 0.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.