drugset / Trial / NCT00245466

Study Investigating the Long-Term Safety and Tolerability of Repeated Doses of Degarelix in Prostate Cancer Patients

NCT00245466

Phase 2 Terminated 88 enrolled Ferring Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

To investigate the long-term safety and tolerability of repeated doses of degarelix to prostate cancer patients

Timeline

Start
2001-10
Primary completion
2006-03
Completion
2006-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Degarelix Other / unclassified 20 mg Subcutaneous
Subject Degarelix Other / unclassified 40 mg Subcutaneous

Indications