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STUDIO RANDOMIZZATO, IN DOPPIO CIECO, CONTROLLATO VERSUS PLACEBO, MULTICENTRICO, DI FASE III, DI VALUTAZIONE DELL’EFFICACIA E DELLA SICUREZZA D’IMPIEGO DI RUXOLITINIB NEI PAZIENTI CON MIELOFIBROSI IN FASE PRECOCE CON MUTAZIONI AD ELEVATO RISCHIO MOLECOLARE. Codice Studio: CINC424A2353 – Rete Ematologica Lombarda

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Project Description

Patologia mielofibrosi
Sponsor Novartis
Farmaco Ruxolitinib
Fase 3
Linea -

 

Codice studio CINC424A2353
Obiettivo primario Valutare l’effetto di Ruxolitinib, nel ritardare la progressione di malattia mielofibrotica.

 

Responsabile della sperimentazione Prof. Francesco Passamonti
ASST dei Sette Laghi, Ospedale di Circolo e Fondazione Macchi
Medici referenti Dr.ssa Domenica Caramazza, Dr.ssa Margherita Maffioli, Dr.ssa Barbara Mora

 

Data inizio dello studio Settembre 2016
Durata dello studio 6 anni
Stato del protocollo Arruolamento APERTO

 

Persona da contattare per l’invio di pazienti
e modalità di contatto
Prof.Francesco Passamonti
francesco.passamonti@asst-settelaghi.it

SCARICA LA SINOSSI DELLO STUDIO

Project Details