{"id":27307,"date":"2026-05-06T06:50:50","date_gmt":"2026-05-06T06:50:50","guid":{"rendered":"https:\/\/www.neuraxpharm.com\/it\/?page_id=27307"},"modified":"2026-05-06T06:54:10","modified_gmt":"2026-05-06T06:54:10","slug":"efficacia-provata","status":"publish","type":"page","link":"https:\/\/www.neuraxpharm.com\/it\/portafoglio\/sclerosi-multipla\/efficacia-provata\/","title":{"rendered":"Efficacia provata"},"content":{"rendered":"\t\t
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\n\t\t\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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Home<\/a><\/div>\n\t\t<\/div>\n\t\t<\/div>\n\t\t<\/div><\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tBRIUMVI\u00ae is where efficacy meets efficiency for patients with relapsing MS\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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Riduzione significativa delle ricadute (endpoint primario)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Soppressione quasi completa delle lesioni


<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Progressione e miglioramento della disabilit\u00e0<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Aumento della percentuale di pazienti senza evidenza di attivit\u00e0 di malattia (NEDA)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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Il primo anti-CD20 a raggiungere un ARR <0,1 in 2 studi clinici di fase 3\n2<\/sup><\/p>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Negli studi clinici di ULTIMATE I e II, BRIUMVI\u00ae ha ridotto significativamente i tassi di ricaduta rispetto a teriflunomide a 96 settimane4<\/sup><\/p>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\t\t\t\tEndpoint finale primario:<\/strong> ARR\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tMeno di 1 ricaduta<\/span> per ogni 12 anni-paziente con BRIUMVI\u00ae nello studio di ULTIMATE Ia,b<\/sup>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tMeno di 1 ricaduta<\/span> per ogni 11 anni-paziente con BRIUMVI\u00ae nello studio di ULTIMATE IIa,b<\/sup>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\"\"\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\ta<\/sup>ARR per BRIUMVI\u00ae osservato negli studi di fase 3 di ULTIMATE I e II. I confronti tra gli studi non sono appropriati a causa della variazione delle popolazioni di pazienti analizzati nei diversi studi.2<\/sup>\n\nb<\/sup>Gli anni-paziente sono stati calcolati sulla base degli ARR medi della popolazione mITT (1\/0,08 = 12,5 e 1\/0,09 = 11,1).2\nSulla base della popolazione mITT modificata e post basale.2<\/sup>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tUn maggior numero di pazienti liberi da ricadute con BRIUMVI\u00ae nei 2 studi clinici1<\/sup>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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Percentuale di pazienti liberi da ricadute a 96 settimane.<\/p>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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BRIUMVI\u00ae ha mostrato una soppressione delle lesioni T1Gd+ rispetto alla teriflunomide1,2<\/sup><\/p>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\t\t\t\tLe lesioni T1 Gd+ sono state soppresse del 97% rispetto a teriflunomide\u00a01,2<\/sup>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tEndpoint finale secondario: lesioni T1 Gd+ alla settimana 96<\/strong>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tBasato sulla popolazione MRI-mITT (pazienti mITT che hanno una risonanza magnetica basale e post basale).\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tLa soppressione delle lesioni T2 nuove o in espansione \u00e8 stata del 92% in ULTIMATE I e del 90% in ULTIMATE II rispetto a teriflunomide1,2<\/sup>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tEndpoint secondario: lesioni T2 nuove o in aumento alla settimana 96<\/strong>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tBasato sulla popolazione MRI-mITT (pazienti mITT che hanno una risonanza magnetica basale e post basale).\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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Gli studi ULTIMATE I e II hanno evidenziato la progressione della disabilit\u00e0 nei pazienti a 12 settimane 1,2<\/sup>\n<\/p>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\t\t\t\tIl 95% dei pazienti negli studi ULTIMATE I e II non ha avuto una progressione confermata della disabilit\u00e0 (CDP) a 12 settimane e >95% dei pazienti non ha avuto una CDP a 24 settimane 1,2\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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\n\t\t\t\t\t\t\t\t\tAnalisi combinata predefinita:<\/strong> CDP\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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Sulla base delle stime di Kaplan-Meier e della popolazione mITT.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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