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Transperineal Intraprostatic Injection of PRX302 Under Ultrasound Guidance for Management of Prostatic Hyperplasia — TRIUMPH-1  

Benign Prostatic Hyperplasia Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled Phase II Study of Transperineal Intraprostatic Injection of PRX302 for the Treatment of Benign Prostatic Hyperplasia

Clinical Trial Summary

The purpose of this study is to determine whether PRX302 is safe and effective in the treatment of moderate to severe Benign Prostatic Hyperplasia (BPH).

Clinical Trial Description

This is a randomized, double-blinded, placebo-controlled study of transperineal intraprostatic injection of PRX302 under sonographic guidance. Subjects will be randomly assigned to the two treatment groups in a ratio of 2:1 between PRX302 and Placebo, stratified by prostate size and baseline IPSS. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00889707
Study type Interventional
Source Sophiris Bio Corp
Contact
Status Completed
Phase Phase 2
Start date January 2009
Completion date September 2010
View Details
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