drugset / Trial / NCT00918983

Clinical Evaluation of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH)

NCT00918983

Phase 3 Completed 500 enrolled Nymox Corporation
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will evaluate the safety and efficacy of a 2.5 mg dose of NX-1207 for the treatment of BPH (benign prostatic hyperplasia) as compared to placebo.

Timeline

Start
2009-04
Primary completion
2013-11
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject FEXAPOTIDE Protein / enzyme biologic 2.5 mg Other