A Study of Docetaxel Plus Carboplatin in Patients With Hormone Refractory Prostate Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

January 31, 2004

Primary Completion Date

April 30, 2006

Study Completion Date

September 30, 2009

Conditions
Prostate Cancer
Interventions
DRUG

Docetaxel

Given intravenously over 2-3 hours once every three weeks. Participant can continue to receive treatment as long as there is no disease progression or serious side effects.

DRUG

Carboplatin

Given intravenously over 2-3 hours once every three weeks. Participant can continue to receive treatment as long as there is no disease progression or serious side effects.

Trial Locations (6)

97239

Oregon Health and Science University, Portland

02114

Massachusetts General Hospital, Boston

02115

Dana-Farber Cancer Institute, Boston

02215

Beth Israel Deaconess Medical Center, Boston

01854

Lowell General Hospital, Lowell

03820

Wentworth Douglass Hospital, Dover

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Bristol-Myers Squibb

INDUSTRY

collaborator

Beth Israel Deaconess Medical Center

OTHER

collaborator

Lowell General Hospital

OTHER

collaborator

Massachusetts General Hospital

OTHER

collaborator

Oregon Health and Science University

OTHER

collaborator

Wentworth-Douglass Hospital

OTHER

lead

Dana-Farber Cancer Institute

OTHER