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STUDIO MULTICENTRICO DI FASE 2 PER VALUTARE ATTIVITÀ E SICUREZZA DI IBRUTINIB ASSOCIATO A RITUXIMAB IN PRIMA LINEA NEI PAZIENTI UNFIT AFFETTI DA LEUCEMIA LINFOCITICA CRONICA (LLC). Codice Studio: LLC1114 – Rete Ematologica Lombarda

STUDIO MULTICENTRICO DI FASE 2 PER VALUTARE ATTIVITÀ E SICUREZZA DI IBRUTINIB ASSOCIATO A RITUXIMAB IN PRIMA LINEA NEI PAZIENTI UNFIT AFFETTI DA LEUCEMIA LINFOCITICA CRONICA (LLC). Codice Studio: LLC1114


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Project Description

Patologia leucemia linfatica cronica
Sponsor GIMENA
Farmaco Ibrutinib+Rituximab
Fase 2
Linea prima

 

Codice studio GIMENA LLC1114
EudraCT number 2014-002714-23
Clinical Trial Number NCT02232386
Obiettivo primario Valutare l’attività del trattamento di prima linea con Ibrutinib associato a Rituximab nei pazienti unfit affetti da LLC in termini di Progression Free Survival (PFS) a dodici mesi.

 

Responsabile della sperimentazione Prof. Robin Foà
study coordinator, GIMEMA Roma
Medici referenti Dr.ssa Ester M. Orlandi
Fondazione IRCCS Policlinico San Matteo Pavia - SC Ematologia

 

Data inizio dello studio 2015
Durata dello studio 90 mesi
Stato del protocollo Arruolamento di 156 pazienti: APERTO

 

Persona da contattare per l’invio di pazienti
e modalità di contatto		 Dr.ssa Ester M.Orlandi
e.orlandi@smatteo.pv.it

SCARICA LA SINOSSI DELLO STUDIO

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