drugset / Trial / NCT01446991

Feasibility and Toxicity of Degarelix for Prostate Downsizing Prior to Permanent Seed Prostate Brachytherapy

NCT01446991

Phase 2 Completed 50 enrolled British Columbia Cancer Agency
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will investigate the efficacy of Degarelix, a Luteinizing Hormone Releasing Hormone (LHRH) antagonist, to reduce prostate volume prior to permanent seed prostate brachytherapy. There are 2 eligible populations of men, all of whom will have selected brachytherapy as their treatment of choice for their prostate cancer. Either they have an enlarged prostate that requires size reduction to render brachytherapy technically feasible, or they require androgen ablation in conjunction with brachytherapy for optimal tumor control. The hypothesis is that Degarelix will provide \> 30% volume reduction by 3 months in \> 30% of men.

Timeline

Start
2012-04
Primary completion
2017-02
Completion
2017-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Degarelix Other / unclassified 80 mg

Indications