Firmagon (Degarelix) Intermittent Therapy
- Registration Number
- NCT01512472
- Lead Sponsor
- Canadian Urology Research Consortium
- Brief Summary
Men with localized prostate cancer requiring intermittent androgen deprivation therapy for biochemical recurrence following radical therapy will be asked to participate in a phase 4 safety and efficacy clinical trial comparing 10 months versus 4 months of degarelix (Firmagon®) therapy with the endpoint of prolonging the off treatment interval.
- Detailed Description
This is an open-label, multi-centre, randomised trial with subjects receiving subcutaneous (s.c.) monthly injections of degarelix depot. All patients will be treated with a one-month starting dose of 240mg on Day 0. Subjects are then randomized to receive either nine or three maintenance doses of one month duration. The primary objective is to determine the effect of degarelix therapy on the length of the off treatment interval (defined as serum Prostate-specific antigen (PSA) increasing to 5 ng/ml) following completion of the androgen deprivation therapy. The trial will also assess the effect of degarelix therapy on PSA kinetics (specifically PSA doubling time), PSA nadir, and effect on quality of life as well as other measures. The efficacy and safety of these two treatments will also be reported.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Male
- Target Recruitment
- 144
- histologically confirmed adenocarcinoma of the prostate for which intermittent endocrine treatment therapy is indicated
- PSA level meeting both of these criteria:
- PSA level of ≥ 5 ng/mL.
- For patients with recurrence after radiotherapy or cryotherapy: Patients should have a serum PSA (two measurements) to be >2 ng/mL higher than a previously confirmed PSA nadir.
- screening serum testosterone level above the lower limit of normal range defined as >2.2 ng/mL.
- Has had previous or is currently under hormonal management of prostate cancer (surgical castration or other hormonal manipulation)
- Has received therapy with the 5-alpha reductase inhibitors finasteride or dutasteride within 12 weeks and 25 weeks, respectively, prior to screening
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 10 month degarelix therapy degarelix - 4 month degarelix therapy arm degarelix -
- Primary Outcome Measures
Name Time Method serum PSA approximately 15 months The study will compare the length of the off treatment interval (in months) of subjects in the 4 month arm vs those in the 10 month arm. The off treatment interval is defined as the time from PSA nadir following completion of hormone therapy in both arms until the time PSA reaches 5.0ng/ml
- Secondary Outcome Measures
Name Time Method serum PSA at 4 months (4 mon arm) or 10 montths (10 mon arm) PSA nadir is described as the serum PSA value after the completion of either 4 months or 10 months of therapy.
Trial Locations
- Locations (15)
Ultra-Med Research
🇨🇦Pointe Claire, Quebec, Canada
The Prostate Centre
🇨🇦Vancouver, British Columbia, Canada
Centre of Clinical Research
🇨🇦Halifax, Nova Scotia, Canada
University Health Network
🇨🇦Toronto, Ontario, Canada
The Urology Specialists / Les Urologues Specialises
🇨🇦Montreal, Quebec, Canada
MUHC Montreal General Hospital
🇨🇦Montreal, Quebec, Canada
McMaster Institute of Urology
🇨🇦Hamilton, Ontario, Canada
Centre of Applied Urological Research / Kingston General Hospital
🇨🇦Kingston, Ontario, Canada
London Health Sciences Centre
🇨🇦London, Ontario, Canada
Northeast Cancer Centre, Health Sciences North
🇨🇦Sudbury, Ontario, Canada
Sunnybrook Health Sciences Centre
🇨🇦Toronto, Ontario, Canada
Recherches Clinique /Clinical Research
🇨🇦Granby, Quebec, Canada
Centre de recherche du CHUQ-L'hotel-Dieu de Quebec
🇨🇦Quebec, Canada
Manitoba Prostate Centre
🇨🇦Winnipeg, Manitoba, Canada
URLX Corporation
🇨🇦Ottawa, Ontario, Canada