Phase III, comparative, multicenter, randomized, controlled, double-blind and superiority research, comparing rituximab-based regimen with conventional therapeutic strategy for the induction of remission in patients with eosinophilic granulomatosis with polyangiitis (EGPA). Patients with newly diagnosed or relapsing EGPA will be randomized in a 1:1 ratio to receive: * Experimental therapeutic strategy based on the use of rituximab (experimental group) * Conventional therapeutic strategy based on Five-Factor Score (FFS)-assessed disease severity (comparative group)
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The percentage of patients who obtained a BVAS=0 and prednisone dose ≤7.5 mg/day at day 180.
Timeframe: 180 days