Extension Study Investigating the Long-Term Safety of Degarelix One-Month Depots in Patients With Prostate Cancer

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

57

Participants

Timeline

Start Date

March 31, 2005

Primary Completion Date

September 30, 2009

Study Completion Date

November 30, 2009

Conditions
Prostate Cancer
Interventions
DRUG

Degarelix

Drug supplied as a powder to be dissolved in the solvent for solution for injection. Degarelix given by subcutaneous injection every 28 days until the end of the study.

Trial Locations (22)

16801

State College Urologic Association, State College

23235

Virginia Urology Center, Richmond

27401

The Urology Center, Greensboro

33180

South Florida Medical Research, Aventura

33907

SW Florida Urological Associates, Fort Myers

35209

Urology Centers of Alabama, Homewood

46825

Northeast Indiana Research, LLC, Fort Wayne

71106

Regional Urology, Shreveport

78229

Urology San Antonio Research, San Antonio

80210

Urology Associate PC', Denver

90505

Western Clinical Research, Torrance

91356

West Coast Clinical Research, Tarzana

92801

Advanced Urology Medical Center, Anaheim

98166

Investigational site, Seattle

08648

Lawrenceville Urology, Lawrenceville

02904

University Urological Research Institute, Providence

05403

University of Vermont, Dept of Surgery, South Burlington

V8T5G1

Can-Med Clinical Research, Inc., Victoria

L4M7G1

The Male and Female Health and Research Centers, Barrie

N3R4N3

Brantford Urology Research, Brantford

L7N3V2

Burlington Professional Care, Burlington

L6H3P1

The Female/Male Health Centres, Oakville

Sponsors
All Listed Sponsors
lead

Ferring Pharmaceuticals

INDUSTRY