Study Investigating the Pharmacokinetics, Pharmacodynamics and Safety of FE200486

PHASE2CompletedINTERVENTIONAL
Enrollment

82

Participants

Timeline

Start Date

April 30, 2002

Primary Completion Date

January 31, 2004

Study Completion Date

January 31, 2004

Conditions
Prostate Cancer
Interventions
DRUG

Degarelix

One dose (2 x 2 mL) of degarelix 40 mg (10 mg/mL), subcutaneous injection.

DRUG

Degarelix

One dose (2 x 2 mL) of degarelix 80 mg (20 mg/mL), subcutaneous injection.

DRUG

Degarelix

One dose (2 x 2 mL) of degarelix 120 mg (30 mg/mL), subcutaneous injection.

DRUG

Degarelix

One dose (2 x 2 mL) of degarelix 160 mg (40 mg/mL), subcutaneous injection.

Trial Locations (12)

20770

Drs. Werner, Murdock & Francis, PA, Greenbelt

33710

Pinellas Urology, Inc., St. Petersburg

33907

SW Florida Urological Associates, Fort Myers

74104

Urology Specialists of Oklahoma, Inc., Tulsa

75231

Urology Clinics of NorthTexas, PA, Dallas

78229

Urology San Antonio Research, San Antonio

80210

Urology Associate PC', Denver

89511

Nevada Urology Associates, Reno

90505

Western Clinical Research, Torrance

92404

San Bernardino Urological Associates Medical Group, San Bernardino

92653

South Orange County Medical Research Center, Laguna Woods

92801

Advanced Urology Medical Center, Anaheim

Sponsors
All Listed Sponsors
lead

Ferring Pharmaceuticals

INDUSTRY