Phase IV Study to Evaluate Bone Mineral Density in No-bone Metastatic Prostate Cancer Treated With Degarelix

PHASE4UnknownINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

June 26, 2017

Primary Completion Date

March 31, 2019

Study Completion Date

March 31, 2020

Conditions
Prostate Cancer
Interventions
DRUG

Degarelix

"Degarelix (Firmagon®) will be administered as a subcutaneous injection in the abdominal region every 28 days, in according to the following schedule:~* Starting dose: 240 mg administered as two consecutive subcutaneous injections of 120 mg each (2 x 3 mL injections).~* Maintenance dose: 80 mg administered as one subcutaneous injection of 80 mg (1 x 4 mL injection).~Treatment will be continued till clinically indicated or till disease progression."

Trial Locations (1)

25123

RECRUITING

Clinical Department of Urology, university Hospital Spedali Civili di Brescia, Brescia

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Ferring Pharmaceuticals

INDUSTRY

lead

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

OTHER