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STUDIO MULTICENTRICO PER VALUTARE L’ATTIVITÀ ANTIVIRALE DI UN TRATTAMENTO SENZA INTERFERONE CON SOFOSBUVIR PIÙ LEDIPASVIR CON O SENZA RIBAVIRINA (GENOTIPI 1, 3 E 4) E SOFOSBUVIR PIÙ RIBAVIRINA (GENOTIPO 2) IN PAZIENTI AFFETTI DA LINFOMA INDOLENTE A CELLULE B ASSOCIATO AD INFEZIONE DA VIRUS DELL’EPATITE C. Codice Studio: FIL-BArT – Rete Ematologica Lombarda

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Project Description

Patologia Linfoma Indolente a cellule B associato a HCV
Sponsor FIL
Farmaco Sofosbuvir/Ledipasvir (+ Ribavirina) ; Sofosbuvir/Ribavirina
Fase 2
Linea Prima

 

Codice studio FIL-BArT
Obiettivo primario Valutare l’efficacia della terapia di combinazione Sofosbuvir/Ledipasvir (+ Ribavirina) e Sofosbuvir/Ribavirina.

 

Responsabile della sperimentazione Prof. Francesco Passamonti
ASST dei Sette Laghi, Ospedale di Circolo e Fondazione Macchi
Medici referenti Dr. Michele Merli

 

Data inizio dello studio 2016
Durata dello studio Due 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