41
Participants
Start Date
September 30, 2008
Primary Completion Date
December 31, 2010
Study Completion Date
December 31, 2013
AV-299
AV-299 monotherapy will be given as intravenous infusion in dose-escalation cohorts at 2, 5, 10, and 20 mg/kg. Once the RP2D has been determined the cohort may be expanded to include up to 12 patients for safety assessment and enriched with up to 12 additional Multiple Myeloma patients.
AV-299 + erlotinib
AV-299 will be given as intravenous infusion at RP2D in combination with erlotinib (150 mg daily). Once the combination-RP2D has been determined the cohort may be expanded to include up to 12 additional patients.
Investigational Site 2, Scottsdale
Investigational Site 3, Columbus
Investigational Site 1, San Antonio
Lead Sponsor
AVEO Pharmaceuticals, Inc.
INDUSTRY