14
Participants
Start Date
March 31, 2013
Primary Completion Date
December 31, 2016
Study Completion Date
December 31, 2016
NGR-hTNF
NGR-hTNF: 0.8 mcg/m² as 60 minutes intravenous infusion every week until confirmed evidence of disease progression or unacceptable toxicity occurs
Pegylated liposomal doxorubicin
50 mg/m² iv every 4 weeks until confirmed evidence of disease progression
Doxorubicin
60 mg/m² iv every 3 weeks for a maximum of 8 cycles
Ospedale San Raffaele, Milan
Fondazione IRCCS Istituto Nazionale dei Tumori, Milan
Istituto Europeo di Oncologia, Milan
"Istituto Nazionale Tumori IRCCS Fondazione Giovanni Pascale", Naples
Lead Sponsor
AGC Biologics S.p.A.
INDUSTRY