Clinical Study of SU011248 in Subjects With High Risk Prostate Cancer Who Have Elected to Undergo Radical Prostatectomy

PHASE1CompletedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

June 30, 2006

Primary Completion Date

July 31, 2009

Conditions
Prostate Cancer
Interventions
DRUG

SU011248

5 Subjects will receive 50.0 mg/d of the study drug for 2 weeks.

DRUG

SU011248

5 Subjects will receive 50.0 mg/d of the study drug for 4 weeks.

DRUG

SU011248

5 Subjects will receive 50.0 mg/d of the study drug for 1 week.

DRUG

SU011248

5 Subjects will receive 37.5 mg/d of the study drug for 1 week.

DRUG

SU011248

5 Subjects will receive 37.5 mg/d of the study drug for 2 weeks.

Trial Locations (1)

90095

University of California, Los Angeles, Jonsson Comprehensive Cancer Center, Los Angeles

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Pfizer

INDUSTRY

lead

Jonsson Comprehensive Cancer Center

OTHER

NCT00790595 - Clinical Study of SU011248 in Subjects With High Risk Prostate Cancer Who Have Elected to Undergo Radical Prostatectomy | Biotech Hunter | Biotech Hunter