drugset / Trial / NCT00743184

Trial of the Safety and Efficacy of Ozarelix in Participants With Benign Prostatic Hyperplasia (BPH)

NCT00743184

Phase 2 Terminated 28 enrolled Spectrum Pharmaceuticals, Inc
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multi-center, randomized, double-blind, placebo-controlled study to evaluate the efficacy of ozarelix compared to placebo in the treatment of lower urinary tract symptoms (LUTS) secondary to benign prostatic hyperplasia (BPH) in men as assessed by the International Prostate Symptom Score (IPSS) at Week 14.

Timeline

Start
2008-12-04
Primary completion
2010-01-20
Completion
2010-01-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Ozarelix Protein / enzyme biologic 15 mg
Subject Ozarelix Protein / enzyme biologic 30 mg