drugset / Trial / NCT01512472

Firmagon (Degarelix) Intermittent Therapy

NCT01512472

RandomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2012-01
Primary completion
2018-01
Completion
2018-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Degarelix Other / unclassified 80 mg Subcutaneous

Indications