RecruitingNot ApplicableNCT03290456

Evaluate the Remission MAINtenance Using Extended Administration of Prednisone in Systemic Anti-neutrophil Cytoplasmic Antibodies (ANCA)-Associated Vasculitis.

A Prospective, Multicentric, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Remission MAINtenance Using Extended Administration of Prednisone in Systemic Anti-neutrophil Cytoplasmic Antibodies (ANCA)-Associated Vasculitis.


Sponsor

Hospices Civils de Lyon

Enrollment

146 participants

Start Date

Aug 20, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

Immunosuppressive therapy of granulomatosis with polyangiitis (GPA, Wegener's) and microscopic polyangiitis (MPA) has transformed the outcome from death to a strong likelihood of disease control and temporary remission. However, most patients have recurrent relapses that lead to damage and require repeated treatment associated with long-term morbidity and death. Rituximab has been shown to be as effective as cyclophosphamide to induce remission and maintenance of remission in severe GPA and MPA patients, with an acceptable safety profile . Although rituximab is becoming the standard of care for maintenance therapy in these patients, relapse still occurs and the optimal duration of prednisone therapy remains debated. On the one hand, most US studies use early withdrawal (6-12 months) because of feared side effects. On the other hand, most European trials propose late withdrawal (\>18 months) given a lower observed relapse rate on long-term low dose glucocorticoids treatment. In a systematic review and meta-analysis, glucocorticoids regimen was the most significant variable explaining the variability between the proportions of ANCA-associated vasculitis patients with relapses. Nevertheless, it was an indirect estimation of treatment effect because of the absence of dedicated randomized trial. This meta-analysis concluded that combined longer-term (i.e. \>12 months) use of low dose prednisone or nonzero glucocorticoids target is associated with a 20% reduction of relapse compared to early withdrawal (i.e. ≤12 months). The relapse rate in patients with early glucocorticoids (10-12 months) withdrawal was provided in two studies and was of 37 and 34%, respectively. By contrast, the relapse rate in patients with late prednisone withdrawal (18-24 months) and receiving rituximab as maintenance treatment was 14% at 24 months in the MAINRITSAN trial. Of note, the decision to withdraw glucocorticoids after 18 months was left to physician's discretion in this study and two thirds of the nonsevere relapses occurred when patients were off prednisone. The trial detailed here is the first prospective trial evaluating the length of glucocorticoid administration as remission adjunctive treatment for patients with GPA or MPA.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Placebo 5mg/day extended of 12 additionnal months. and a drug called Prednisone 5mg/day extended of 12 additional months for people with granulomatosis with polyangitis. The study is currently recruiting participants at 45 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPrednisone 5mg/day extended of 12 additional months

Prednisone 5mg/day orally during 12 Month + 1 mg/week tapering until 0mg.

DRUGPlacebo 5mg/day extended of 12 additionnal months.

1mg/week orally tapering Prednisone until Month 1 + Placebo orally 5mg/day until Month 13


Locations(45)

CHU Amiens-Hôpital Nord

Amiens, France

CHU Angers

Angers, France

Clinique Rhône-Durance

Avignon, France

Hôpital Jeanne d'Arc

Bar-le-Duc, France

Hôpital Avicenne

Bobigny, France

Hôpital La Cavale Blanche

Brest, France

Hôpital Louis Pradel

Bron, France

CHU de Caen - Cote de Nacre

Caen, France

Hôpital Louis Pasteur

Chartres, France

CHU Estaing

Clermont-Ferrand, France

CHU Gabriel Montpied

Clermont-Ferrand, France

CHIC Créteil

Créteil, France

CHRU François Mitterrand

Dijon, France

CHRU François Mitterrand

Dijon, France

CHRU Lille - Hôpital Claude Huriez

Lille, France

Centre Hospitalier Croix Rousse

Lyon, France

Hôpital Edouard Herriot

Lyon, France

Hôpital Edouard Herriot

Lyon, France

Hôpital de la Conception

Marseille, France

Hôpital de la Conception

Marseille, France

Hôpital La Timone

Marseille, France

HP Site Belle Isle

Metz, France

CHU Nantes - Hôtel Dieu

Nantes, France

CHU de Nice - Hôpital Pasteur 2

Nice, France

Hôpital la Pitié Salpêtrière

Paris, France

Hôpital Cochin

Paris, France

Hôpital Européen G. Pompidou

Paris, France

Hôpital Saint Louis

Paris, France

Hôpital Haut Lévêque

Pessac, France

Centre Hospitalier Lyon Sud

Pierre-Bénite, France

CH Lyon Sud

Pierre-Bénite, France

CH Lyon Sud

Pierre-Bénite, France

CHU de Poitiers

Poitiers, France

CHRU Rennes - Hôpital Sud

Rennes, France

Hôpital Charles Nicolle

Rouen, France

CHU Strasbourg

Strasbourg, France

CHRU Hautepierre

Strasbourg, France

Hopitaux Universaitaire de Strasbourg Hopitaux

Strasbourg, France

Hôpital Foch

Suresnes, France

CHRU Bretonneau

Tours, France

CH de Troyes

Troyes, France

CH Valenciennes

Valenciennes, France

Hôpitaux de Brabois

Vandœuvre-lès-Nancy, France

CH Bretagne Atlantique

Vannes, France

CH de Verdun

Verdun, France

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NCT03290456