drugset / Trial / NCT00819156

Dose Finding Trial With a New Treatment (Degarelix) for Prostate Cancer

NCT00819156

Phase 2 Completed 189 enrolled Ferring Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the trial was to evaluate the safety and efficacy of degarelix when comparing six different doses. The patients participating in the trial were treated with degarelix every month for a year. During the treatment the patients had to visit the clinic for investigations. Blood samples for testosterone, dihydrotestosterone, luteinizing hormone, follicle stimulating hormone, and Prostate Specific Antigen were taken and analysed throughout the trial.

Timeline

Start
2004-02
Primary completion
2005-06
Completion
2005-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Degarelix Other / unclassified 80 mg Subcutaneous
Subject Degarelix Other / unclassified 120 mg Subcutaneous
Subject Degarelix Other / unclassified 160 mg Subcutaneous

Indications