7
Participants
Start Date
August 31, 2012
Primary Completion Date
May 31, 2015
Study Completion Date
May 31, 2015
AUY922
AUY922 will be administered as an intravenous infusion over 60 minutes, on a once weekly schedule. A cycle on study will be defined as 28 days. The dose to be studied are 70 mg/m2 and 55 mg/m2 if DLTs are identified in the first 3-6 patients. The same schedule of administration will be used for all patients in this trial.
Memorial Sloan Kettering Cancer Center, New York
Collaborators (1)
Novartis
INDUSTRY
Memorial Sloan Kettering Cancer Center
OTHER