Panitumumab in Cetuximab Refractory KRAS Wild-Type Colorectal Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

May 31, 2009

Primary Completion Date

December 31, 2011

Study Completion Date

December 31, 2011

Conditions
Colorectal Cancer
Interventions
DRUG

panitumumab

Panitumumab is administered intravenously (IV) by an infusion pump through a peripheral line or indwelling catheter using a 0.2 or 0.22-micron in-line filter infusion set-up over 1 hour 15 minutes. The starting panitumumab dose is 6 mg/kg administered every 14 days for as long as patients are on study without evidence of disease progression or demonstrating intolerance to treatment. The total dose may be rounded up or down by no greater than 10 mg. The panitumumab dose will be calculated based on the subject's actual body weight at each visit. Panitumumab will be diluted in a minimum of 100 mL of pyrogen-free 0.9% sodium chloride solution (normal saline solution, supplied by the site). The maximum concentration of the diluted solution to be infused should not exceed 10 mg/mL.

Trial Locations (3)

02115

Beth Israel Deaconess Medical Center, Boston

Dana-Farber Cancer Institute, Boston

02214

Massachusetts General Hospital, Boston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Beth Israel Deaconess Medical Center

OTHER

collaborator

Dana-Farber Cancer Institute

OTHER

collaborator

Amgen

INDUSTRY

lead

Massachusetts General Hospital

OTHER

NCT00842257 - Panitumumab in Cetuximab Refractory KRAS Wild-Type Colorectal Cancer | Biotech Hunter | Biotech Hunter