20
Participants
Start Date
February 28, 2011
Primary Completion Date
May 31, 2015
Study Completion Date
May 31, 2015
AUY922
Weekly intravenous infusion on Day 1, 8, 15 and 22 of each 28 day cycle until unacceptable toxicity develops or disease progression. A minimum of 3 patients will be enrolled into each cohort. The anticipated dose escalation sequence of AUY922 is 40, 55, and 70 mg/m2 will be used.
Cetuximab
Cetuximab will be administered after each AUY922 infusion, intravenously on Day 1, 8, 15 and 22 of each 28 day cycle until unacceptable toxicity develops or disease progression.
Swedish Medical Center Cancer Institute, Seattle
Collaborators (1)
Novartis Pharmaceuticals
INDUSTRY
Swedish Medical Center
OTHER