9
Participants
Start Date
January 31, 2014
Primary Completion Date
January 31, 2015
Study Completion Date
September 30, 2015
Oprozomib
Study subjects will receive oprozomib administered orally.
Melphalan
Study subjects will receive melphalan 9 mg/m2.
Prednisone
Study subjects will receive prednisone 60 mg/m2.
Department of Clinical Therapeutics, University of Athens, Athens
Ospedale Oncologico Regionale, Rionero in Vulture
Azienda Ospedaliera Universitaria S Martino, Genova
AOU Maggiore della Carita, SCDU Heamatology, Novara
University of Rome, Rome
Hospital City of Health and Science of Turin, Hematology 1 Division, Turin
Vrijc Universiteit Medisch Centrum, Department of Hematology, Amsterdam
Erasmus MC, Department of Hematology, Rotterdam
Lead Sponsor
Amgen
INDUSTRY