A Phase 1 Dose-Escalation Study in Advanced Solid Tumors, Lymphomas or Multiple Myeloma

PHASE1CompletedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

September 30, 2008

Primary Completion Date

December 31, 2010

Study Completion Date

December 31, 2013

Conditions
Malignant Solid TumorLymphomasMultiple Myeloma
Interventions
BIOLOGICAL

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.

BIOLOGICAL

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.

Trial Locations (3)

Unknown

Investigational Site 2, Scottsdale

Investigational Site 3, Columbus

Investigational Site 1, San Antonio

Sponsors
All Listed Sponsors
lead

AVEO Pharmaceuticals, Inc.

INDUSTRY