SU011248 in Advanced Hepatocellular Carcinoma

PHASE2CompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

April 30, 2006

Primary Completion Date

November 30, 2007

Study Completion Date

March 31, 2009

Conditions
Hepatocellular CarcinomaLiver Cancer
Interventions
DRUG

SU011248

Patients will receive SU011248 37.5 mg/day for 4 weeks continuously followed by 2 weeks of rest per cycle (each cycle = 6 weeks).

Trial Locations (3)

02114

Massachusetts General Hospital, Boston

02115

Beth Israel Deaconess Medical Center, Boston

Dana-Farber Cancer Institute, Boston

All Listed Sponsors
collaborator

Beth Israel Deaconess Medical Center

OTHER

collaborator

Brigham and Women's Hospital

OTHER

collaborator

Dana-Farber Cancer Institute

OTHER

lead

Massachusetts General Hospital

OTHER

NCT00361309 - SU011248 in Advanced Hepatocellular Carcinoma | Biotech Hunter | Biotech Hunter