Two Doses of Conjugated Estrogen (Premarin) in Patients With Androgen-Independent Prostate Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

March 31, 2003

Primary Completion Date

July 31, 2005

Study Completion Date

June 30, 2011

Conditions
Prostate Cancer
Interventions
DRUG

Premarin

Group A: 1.25mg once a day Group B: 1.25mg three time a day Group A has been closed and participants have been given the option of enrolling in Group B. Treamtment can continue until disease progression or serious side effects.

Trial Locations (3)

02115

Beth Israel Deaconess Medical Center, Boston

Dana-Farber Cancer Insitute, Boston

Massachusetts General Hospital, Boston

All Listed Sponsors
collaborator

Beth Israel Deaconess Medical Center

OTHER

collaborator

Massachusetts General Hospital

OTHER

collaborator

Brigham and Women's Hospital

OTHER

collaborator

Lowell General Hospital

OTHER

collaborator

South Shore Hospital

OTHER

collaborator

Emerson Hospital, Concord, MA

OTHER

collaborator

Saint Anne's Hospital

OTHER

lead

Dana-Farber Cancer Institute

OTHER

NCT00134654 - Two Doses of Conjugated Estrogen (Premarin) in Patients With Androgen-Independent Prostate Cancer | Biotech Hunter | Biotech Hunter