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Clinical Trial Summary

This exploratory study will be conducted open label in a single investigational clinical unit. Altogether 52 patients with benign prostate hyperplasia (BPH) will be randomly assigned to receive 4 different treatments with degarelix.


Clinical Trial Description

The present study aims at exploring the potential of the currently available formulation of degarelix to treat BPH with only a short transient lowering of the serum testosterone concentration to or below the castration level defined as 0.5 ng/mL. Two doses and two dosing regimens (32 and 64 mg administered either as a single administration or as two administrations separated by 14 days) will be evaluated for 42 days. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00527488
Study type Interventional
Source Ferring Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date October 2007
Completion date May 2009

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