Informations générales (source: ClinicalTrials.gov)

NCT03290456 En recrutement IDF
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.
Interventional
  • Vascularite
  • Vascularite systémique
N/A
Hospices Civils de Lyon (Voir sur ClinicalTrials)
août 2019
octobre 2029
02 octobre 2025
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.
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Etablissements

Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données
CHI DE CRETEIL Antoine FROISSART Annulé 29/03/2024 01:28:33  Contacter
HOPITAL FOCH Matthieu GROH En recrutement IDF 04/05/2026 07:25:16  Contacter
Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
AP-HP - Hôpital Avicenne Robin DHOTE, MD Contact (sur clinicalTrials)
AP-HP - Hôpital Cochin Xavier PUECHAL, Pr Contact (sur clinicalTrials)
AP-HP - Hôpital Europeen Georges Pompidou Alexandre KARRAS, Pr Contact (sur clinicalTrials)
HOPITAL FOCH Mathieu GROH, MD Contact (sur clinicalTrials)
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Centre Hospitalier Lyon Sud - 69310 - Pierre-Bénite 2987314 - France Jean-Christophe LEGA, Pr Contact (sur clinicalTrials)
CH Bretagne Atlantique - 56017 - Vannes 2970777 - France Pascal GODMER, MD Contact (sur clinicalTrials)
CH Lyon Sud - 69495 - Pierre-Bénite 2987314 - France Jean Christophe LEGA, Pr Contact (sur clinicalTrials)
CH Valenciennes - 59322 - Valenciennes 2971041 - France Thomas QUEMENEUR, MD Contact (sur clinicalTrials)
CHRU Lille - Hôpital Claude Huriez - 59037 - Lille 2998324 - France Eric HACHULLA, Pr Contact (sur clinicalTrials)
CHRU Rennes - Hôpital Sud - 35200 - Rennes 2983990 - France Thomas LE GALLOU, MD Contact (sur clinicalTrials)
CHU Amiens-Hôpital Nord - 80054 - Amiens 3037854 - France Jean SCHMIDT, MD Contact (sur clinicalTrials)
CHU de Caen - Cote de Nacre - 14033 - Caen 3029241 - France Nicolas MARTIN-SILVA, MD Contact (sur clinicalTrials)
CHU de Nice - Hôpital Pasteur 2 - 06001 - Nice 2990440 - France Nathalie TIEULIE, MD Contact (sur clinicalTrials)
CHU de Poitiers - 86021 - Poitiers 2986495 - France Mathieu PUYADE, MD Contact (sur clinicalTrials)
CHU Gabriel Montpied - 63003 - Clermont-Ferrand 3024635 - France Olivier AUMAITRE, Pr Contact (sur clinicalTrials)
CHU Nantes - Hôtel Dieu - 44093 - Nantes 2990969 - France Antoine NEEL, MD Contact (sur clinicalTrials)
Hôpital de la Conception - 13005 - Marseille 2995469 - France Noémie JOURDE CHICHE, Pr Contact (sur clinicalTrials)
Hôpital La Cavale Blanche - 29200 - Brest 3030300 - France Claire DE MOREUIL, MD Contact (sur clinicalTrials)
Hôpital Louis Pasteur - 28018 - Chartres 3026467 - France Richard DAMADE, MD Contact (sur clinicalTrials)
Hôpitaux de Brabois - 54511 - Vandœuvre-lès-Nancy 2970797 - France Rolland JAUSSAUD, MD Contact (sur clinicalTrials)
Hopitaux Universaitaire de Strasbourg Hopitaux - Strasbourg 2973783 - France Thierry KRUMMEL, MD Contact (sur clinicalTrials)
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Centre Hospitalier Croix Rousse - 69004 - Lyon 2996944 - France Pascal SEVE, Pr Contact (sur clinicalTrials)
CH de Troyes - 10003 - Troyes 2971549 - France Pascale CHAUVEAU-JOUVE, MD Contact (sur clinicalTrials)
CH de Verdun - 55100 - Verdun 2969958 - France Assetou DIARRASOUBA, MD Contact (sur clinicalTrials)
CHIC Créteil - 94010 - Créteil 3022530 - France Antoine FROISSART, MD Contact (sur clinicalTrials)
CHRU Bretonneau - 37044 - Tours 2972191 - France Elisabeth DIOT, MD Contact (sur clinicalTrials)
CHRU François Mitterrand - 21000 - Dijon 3021372 - France Jean-Michel REBIBOU, Pr Contact (sur clinicalTrials)
CHRU Hautepierre - 67098 - Strasbourg 2973783 - France Jacques-Eric GOTTENBERG, Pr Contact (sur clinicalTrials)
CHU Angers - 49933 - Angers 3037656 - France Christian LAVIGNE, MD Contact (sur clinicalTrials)
CHU Estaing - 63003 - Clermont-Ferrand 3024635 - France Marc RUIVARD, Pr Contact (sur clinicalTrials)
CHU Strasbourg - 67000 - Strasbourg 2973783 - France Vincent POINDRON, MD Contact (sur clinicalTrials)
Clinique Rhône-Durance - 84000 - Avignon 3035681 - France Pierre GOBERT, MD Contact (sur clinicalTrials)
Hôpital Charles Nicolle - 76031 - Rouen 2982652 - France Ygal BENHAMOU, MD Contact (sur clinicalTrials)
Hôpital Edouard Herriot - 69137 - Lyon 2996944 - France Laurent JULLIARD, Pr Contact (sur clinicalTrials)
Hôpital Haut Lévêque - 33600 - Pessac 2987805 - France Jean-François VIALLARD, Pr Contact (sur clinicalTrials)
Hôpital Jeanne d'Arc - 55000 - Bar-le-Duc 3034911 - France Philippe EVON, MD Contact (sur clinicalTrials)
Hôpital la Pitié Salpêtrière - 75013 - Paris 2988507 - France Patrice CACOUB, Pr Contact (sur clinicalTrials)
Hôpital La Timone - 13385 - Marseille 2995469 - France Nicolas SCHLEINITZ, Pr Contact (sur clinicalTrials)
Hôpital Louis Pradel - 69500 - Bron 3029931 - France Vincent COTTIN, Pr Contact (sur clinicalTrials)
Hôpital Saint Louis - 75475 - Paris 2988507 - France Alfred MAHR, Pr Contact (sur clinicalTrials)
HP Site Belle Isle - 57045 - Metz 2994160 - France François MAURIER, MD Contact (sur clinicalTrials)

Critères

Tous


- Patients with a diagnosis of MPA or GPA independently of ANCA status,

- Patient aged of 18 years or older,

- Patients with newly-diagnosed disease or relapsing disease at the time of screening,
with an inactive disease defined as a BVAS = 0,

- Patients receiving maintenance infusion of rituximab 500 mg at 6 and 12 months after
the start of vasculitis induction

- Patients receiving 5-10 mg/day of prednisone at screening,

- Patient able to give written informed consent prior to participation in the study.

- At Inclusion visit day, patient must be between 5 and 10 mg/day prednisone and at
randomization visit day (D1), patient must be at 5 mg/day prednisone

Exclusion Criteria:


- Patients with EGPA, or other vasculitides, defined by the ACR criteria and/or the
Chapel Hill Consensus Conference,

- Patients with vasculitis with active disease defined as a BVAS >0,

- Patients with acute infections or chronic active infections (including HIV, HBV or
HCV),

- Patients with active cancer or recent cancer (<5 years), except basocellular
carcinoma and prostatic cancer of low activity controlled by hormonal treatment,

- Pregnant women and lactation. Patients with childbearing potential should have
reliable contraception for the all duration of the study,

- Patients with other uncontrolled diseases, including drug or alcohol abuse, severe
psychiatric diseases, that could interfere with participation in the trial according
to the protocol,

- Patients included in other investigational therapeutic study within the previous 3
months,

- Patients suspected not to be observant to the proposed treatments,

- Patients who have white blood cell count ≤4,000/mm3,

- Patients who have platelet count ≤100,000/mm3,

- Patients who have ALT or AST level greater than 3 times the upper limit of normal
that cannot be attributed to underlying MPA-GPA disease,

- Patients unable to give written informed consent prior to participation in the
study.

- Patients with contraindication to use rituximab,