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STUDIO PROOF OF CONCEPT DI FASE 2 PER VALUTARE DISGIUNTAMENTE L’ATTIVITÀ DI TALACOTUZUMAB (JNJ-56022473) O DARATUMUMAB IN SOGGETTI DIPENDENTI DALLE TRASFUSIONI AFFETTI DA SINDROMI MIELODISPLASTICHE (MDS) CON RISCHIO BASSO O INTERMEDIO-1 RECIDIVANTI O REFRATTARIE AL TRATTAMENTO CON GLI AGENTI STIMOLANTI L’ERITROPOIESI (ESA). Codice Studio: 56022473MDS2002 – Rete Ematologica Lombarda

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Project Description

Patologia Mielodisplasie
Sponsor Janssen-Cilag
Farmaco Daratumumab e Talacotuzumab
Fase 2
Linea -

 

Codice studio 56022473MDS2002
Obiettivo primario Valutare l'efficacia (indipendenza dalle trasfusioni [TI]) di talacotuzumab (JNJ-56022473) o daratumumab in soggetti dipendenti dalle trasfusioni affetti da sindromi mielodisplastiche (MDS) con rischio basso o intermedio-1 recidivanti o refrattarie al trattamento con gli agenti stimolanti l'eritropoiesi.

 

Responsabile della sperimentazione Prof. Matteo Della Porta
Cancer Center - Humanitas Research Hospital – Rozzano, Milano
Medici referenti Dr.ssa Marianna Rossi, Dr.ssa Elisabetta Todisco - Istituto Clinico Humanitas

 

Data inizio dello studio Aprile 2017
Durata dello studio fino a febbraio 2019
Stato del protocollo Arruolamento IN APERTURA

 

Persona da contattare per l’invio di pazienti
e modalità di contatto
Prof.Matteo Della Porta
matteo.della_porta@hunimed.eu

SCARICA LA SINOSSI DELLO STUDIO

Project Details