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STUDIO DI FASE 2, RANDOMIZZATO, MULTICENTRICO, IN APERTO PER VALUTARE L’EFFICACIA E LA SICUREZZA DI AZACITIDINA SOTTOCUTANEA SOMMINISTRATA IN COMBINAZIONE CON DURVALUMAB (MEDI4736) IN SOGGETTI CON SINDROME MIELODISPLASTICA (MDS) AD ALTO RISCHIO NON PRECEDENTEMENTE TRATTATI O IN SOGGETTI ANZIANI (≥ 65 ANNI) CON LEUCEMIA MIELOIDE ACUTA (AML) NON ELEGGIBILI AL TRAPIANTO CON CELLULE STAMINALI EMATOPOIETICHE (HSCT). Codice Studio: MEDI4736-MDS-001 – Rete Ematologica Lombarda

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Project Description

Patologia AML/MDS
Sponsor Celgene Corporation
Farmaco Azacitidina SC + Durvalumab vs Azacididina SC
Fase 2
Linea Prima

 

Codice studio MEDI4736-MDS-001
Obiettivo primario Valutare l’efficacia di azacitidina sottocute associata a Durvalumab, rispetto alla monoterapia con azacitidina sottocute, nella popolazione rappresentata nello studio.

 

Responsabile della sperimentazione Prof. Francesco Passamonti, ASST dei Sette Laghi, Ospedale di Circolo e Fondazione Macchi - Varese
Prof. Luca Malcovati, Fondazione IRCCS Policlinico San Matteo - Pavia

Medici referenti Dr.ssa Claudia Basilico, Dr.ssa Alessandra Stasia - ASST dei Sette Laghi, Ospedale di Circolo e Fond. Macchi
Prof.Luca Malcovati, Dr.ssa Marta Ubezio - Fondazione IRCCS Policlinico San Matteo

 

Data inizio dello studio Settembre 2016
Durata dello studio 15 mesi
Stato del protocollo Arruolamento APERTO

 

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

IRCCS Policlinico San Matteo:
Prof. Luca Malcovati    luca.malcovati@unipv.it
Dr.ssa Marta Ubezio    m.ubezio@smatteo.pv.it

SCARICA LA SINOSSI DELLO STUDIO

Project Details