Study on Continuing or Stopping Immunosuppressive Therapy with Rituximab in Patients with ANCA Vasculitis and End-stage Kidney Disease

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What is this study about?

This clinical trial is focused on studying two diseases: ANCA vasculitis and end-stage renal disease. ANCA vasculitis is a condition where the immune system attacks the blood vessels, leading to inflammation. End-stage renal disease is the final stage of chronic kidney disease, where the kidneys can no longer function properly. The study is investigating the effects of stopping or continuing immunosuppressive therapy in patients with these conditions. Immunosuppressive therapy involves medications that reduce the activity of the immune system to prevent it from attacking the body.

The medications being studied include rituximab, azathioprine, prednisone, and mycophenolate mofetil. Rituximab is given as an injectable solution, while azathioprine, prednisone, and mycophenolate mofetil are taken orally in tablet form. The purpose of the study is to determine if stopping immunosuppressive therapy is better for patients with end-stage renal disease and ANCA vasculitis compared to continuing the standard maintenance therapy. The study will follow participants for 24 months to observe any severe events such as major relapses, severe infections, or death.

Participants in the study will be randomly assigned to either continue their current immunosuppressive therapy or to stop it. The study will monitor the health of the participants over the course of two years to see which approach leads to better outcomes. This research aims to provide valuable information on the best treatment approach for patients with these serious conditions.

1 joining the study

Upon joining the study, the patient is randomly assigned to one of two groups: one group will continue with standard maintenance immunosuppressive therapy, and the other group will discontinue immunosuppressive therapy.

2 medication administration

For patients continuing therapy, medications may include rituximab (injectable solution), azathioprine (oral tablet), prednisolone (oral tablet), mycophenolate mofetil (oral film-coated tablet), and prednisone (oral tablet).

The specific dosage and frequency of these medications will be determined by the study protocol and the patient’s medical condition.

3 monitoring and follow-up

Patients will be monitored regularly to assess their health status and any potential side effects of the treatment.

The primary focus is on the time between randomization and the first severe event, such as a severe infection, major relapse of ANCA vasculitis, or death, over a 24-month follow-up period.

4 evaluation of outcomes

The study aims to evaluate the effectiveness of discontinuing immunosuppressive therapy compared to continuing standard therapy in terms of severe event-free survival over 24 months.

Who Can Join the Study?

  • Age between 18 and 90 years old.
  • Patients with a condition called GPA or MPA AAV, which involves kidney damage.
  • Patients experiencing their first symptoms or a return of AAV.
  • Patients with End-stage Renal Disease (ESRD), which means their kidneys are not working well. This is defined by a specific test result (glomerular filtration rate) of 15 or less, or if they need dialysis for more than 60 days.
  • Patients with ESRD in their original kidneys, not transplanted ones.
  • Patients who have agreed in writing to participate in the study.
  • Patients who are part of the French social security system.

Who Cannot Join the Study?

  • Patients with end-stage renal disease, which means the kidneys are no longer working well enough to meet the body’s needs.
  • Patients with ANCA vasculitis, a condition where the immune system attacks small blood vessels, causing inflammation.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Centre Hospitalier Universitaire De Lille Lille France
Centre Hospitalier Regional Et Universitaire De Brest Brest France
Oncopole Claudius Regaud Toulouse France
University Hospital Of Clermont-Ferrand Clermont Ferrand France
CHU Grenoble Alpes La Tronche France
Centre hospitalier Emile Roux Le Puy-En-Velay France
Hôpital Européen Georges-Pompidou Paris France
Centre Hospitalier Universitaire De Bordeaux Bordeaux France

Other Sites

Site Name City Country Status
Centre Hospitalier Departemental Vendee La Roche sur Yon France
Centre Hospitalier Universitaire Rouen Rouen France
Hopital Tenon Paris France
Centre Hospitalier Universitaire De Montpellier Montpellier France
Centre Hospitalier Universitaire De Nantes Nantes France
Centre Hospitalier Universitaire De Nice Nice France
Centre Hospitalier Universitaire Amiens Picardie Amiens France
Centre Hospitalier Universitaire De Rennes Rennes France
Centre Hospitalier Universitaire De Nimes Nimes France
Centre Hospitalier Lyon Sud Pierre Benite France
Centre Hospitalier D Avignon Avignon France
Centre Hospitalier Intercommunal De Cornouaille Quimper France
Centre Hospitalier Alpes Leman 74130 France
Centre Hospitalier Intercommunal De Mont De Marsan Et Du Pays Des Sources Mont-de-Marsan France
Groupe Hospitalier Rance Emeraude Saint-Malo France
Centre hospitalier de Saint-Nazaire St Nazaire France
Centre Hospitalier Le Mans Le Mans France
Hopital Ambroise Pare Boulogne-Billancourt France
Hopital NOVO Pontoise France
Centre Hospitalier Bretagne Atlantique Vannes France
Centre Hospitalier De Boulogne Sur Mer Boulogne sur Mer France
Groupe Hospitalier De La Region De Mulhouse Et Sud Alsace Mulhouse France
Centre Hospitalier Universitaire De Poitiers Poitiers France
Centre Hospitalier Groupe Hospitalier De La Rochelle Re Aunis La Rochelle France
Les Hopitaux De Chartres Le Coudray France
Centre Hospitalier De Valenciennes Valenciennes France
Aub Sante Saint-Gregoire France
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Cmnewrtj Sjaow Ebokewp Toulouse France
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Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
France France
Not recruiting
01.02.2018

Trial locations

Immunosuppressive Therapy is a treatment used to reduce the activity of the immune system. In this clinical trial, it is used as a standard maintenance therapy for patients with ANCA vasculitis and end-stage renal disease. The goal is to prevent the immune system from attacking the body’s own tissues, which can help manage the symptoms of the disease and prevent further damage to the kidneys.

End-stage Renal Disease – This condition occurs when the kidneys are no longer able to function at a level needed for day-to-day life. It is the final stage of chronic kidney disease, where the kidneys have lost about 90% of their ability to function normally. Patients with this disease often require dialysis or a kidney transplant to survive. The progression involves a gradual decline in kidney function over time, leading to the accumulation of waste products in the body. Symptoms may include fatigue, swelling, and difficulty concentrating. The disease can result from various causes, including diabetes and high blood pressure.

ANCA Vasculitis – This is an autoimmune disease characterized by inflammation of the blood vessels, which can lead to damage in various organs. The condition is associated with the presence of anti-neutrophil cytoplasmic antibodies (ANCA) in the blood. It can affect small to medium-sized blood vessels, leading to symptoms such as fatigue, fever, and weight loss. As the disease progresses, it can cause organ damage, particularly in the kidneys and lungs. The inflammation can lead to reduced blood flow and tissue damage. The exact cause of ANCA vasculitis is not well understood, but it involves an abnormal immune response.

Trial ID:
2024-512470-10-00
Protocol code:
CHD005-17
NCT ID:
NCT03323476
Trial Phase:
Human Pharmacology (Phase I) – Other

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