Efficacy and Safety of Degarelix One Month Dosing Regimen in Korean Patients With Prostate Cancer

PHASE3CompletedINTERVENTIONAL
Enrollment

157

Participants

Timeline

Start Date

March 31, 2010

Primary Completion Date

November 30, 2011

Study Completion Date

November 30, 2011

Conditions
Prostate Cancer
Interventions
DRUG

Degarelix 240/80 mg

The degarelix doses were administered into the abdominal wall every 28 days. A starting dose of 240 mg (40 mg/mL) degarelix was administered on Day 0 as two 3 mL subcutaneous (s.c.) injections. The subsequent maintenance doses of 80 mg (20 mg/mL) degarelix were administered as single 4 mL s.c. injections at 28 day intervals from day 28 to day 168.

Trial Locations (11)

Unknown

Kyoungbuk National University Hospital, Daegu

Hallym University Sacred Heart Hospital, Pyungchon

Pusan National University Yangsan Hospital, Mulgeum-eup

Seoul National University Bundang Hospital, Seongnam

Asan Medical Center, Seoul

Korea University Hospital, Seoul

Samsung Medical Center, Seoul

Seoul National University Hospital, Seoul

Seoul St. Mary's Hospital, Seoul

Yonsei University Health System (Sevrance Hospital), Seoul

Yonsei University Health System Gangnam Sevrance, Seoul

All Listed Sponsors
collaborator

Ferring Pharmaceuticals Korea, Ltd.

OTHER

lead

Ferring Pharmaceuticals

INDUSTRY