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A RANDOMIZED PHASE 2/3 STUDY OF DACOGEN® (DECITABINE) PLUS TALACOTUZUMAB (JNJ-56022473; ANTI-CD123) VERSUS DACOGEN (DECITABINE) ALONE IN PATIENTS WITH AML WHO ARE NOT CANDIDATES FOR INTENSIVE CHEMOTHERAPY. Codice Studio: 56022473AML2002 – Rete Ematologica Lombarda

A RANDOMIZED PHASE 2/3 STUDY OF DACOGEN® (DECITABINE) PLUS TALACOTUZUMAB (JNJ-56022473; ANTI-CD123) VERSUS DACOGEN (DECITABINE) ALONE IN PATIENTS WITH AML WHO ARE NOT CANDIDATES FOR INTENSIVE CHEMOTHERAPY. Codice Studio: 56022473AML2002


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Project Description

Patologia Leucemia Mieloide Acuta
Sponsor Janssen-Cilag
Farmaco Decitabina e Talacotuzumab
Fase 2/3
Linea -

 

Codice studio 56022473AML2002
Obiettivo primario Obiettivo primario: valutazione della percentuale di risposta completa (CR) e la valutazione della sopravvivenza globale (OS) nei pazienti con AML non precedentemente trattata non idonei alla chemioterapia intensiva di induzione e assegnati mediante randomizzazione al trattamento con decitabina + JNJ-56022473 alla dose RP2D o con decitabina in monoterapia.

 

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 15 dicembre 2016
Durata dello studio fino a gennaio 2019
Stato del protocollo Arruolamento APERTO

 

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

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