Firmagon (Degarelix) Intermittent Therapy

PHASE4TerminatedINTERVENTIONAL
Enrollment

144

Participants

Timeline

Start Date

January 31, 2012

Primary Completion Date

January 31, 2018

Study Completion Date

January 31, 2018

Conditions
Prostate Cancer Recurrent
Interventions
DRUG

degarelix

Starting dose of 240 mg (40 mg/mL; injection volume 2 x 3 mL; s.c.) degarelix one-month depot will be administered sc on Day 0, followed by a maintenance dose of 80 mg (20 mg/mL; injection volume 1 x 4 mL; s.c.) sc degarelix one-month depot will be administered into the anterior abdominal wall on Month 1, 2, 3, 4, 5, 6, 7, 8 and 9 for the 10 month arm and month 1, 2 and 3 for the 4 month arm.

Trial Locations (15)

V6Z 3J5

The Prostate Centre, Vancouver

R3E 0V9

Manitoba Prostate Centre, Winnipeg

B3H 1V7

Centre of Clinical Research, Halifax

P3E 5J1

Northeast Cancer Centre, Health Sciences North, Greater Sudbury

L8N 4A6

McMaster Institute of Urology, Hamilton

K7L 3J7

Centre of Applied Urological Research / Kingston General Hospital, Kingston

N6A 5W9

London Health Sciences Centre, London

K1H 1A2

URLX Corporation, Ottawa

M4N 3M5

Sunnybrook Health Sciences Centre, Toronto

M5G 2M9

University Health Network, Toronto

J2G 8Z9

Recherches Clinique /Clinical Research, Granby

H2X 1N8

The Urology Specialists / Les Urologues Specialises, Montreal

H3G 1A4

MUHC Montreal General Hospital, Montreal

H9R 4S3

Ultra-Med Research, Pointe-Claire

G1R 3S1

Centre de recherche du CHUQ-L'hotel-Dieu de Quebec, Québec

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Ferring Pharmaceuticals

INDUSTRY

lead

Canadian Urology Research Consortium

OTHER

NCT01512472 - Firmagon (Degarelix) Intermittent Therapy | Biotech Hunter | Biotech Hunter