drugset / Trial / NCT01846793

Phase 3 Evaluation of Re-Injection of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH)(NX02-0022)

NCT01846793

Phase 3 Completed 160 enrolled Nymox Corporation
NaSingle-groupOpen-labelTreatment

Summary

This study is designed to demonstrate the safety and efficacy of a second transrectal intraprostatic injection of NX-1207 given to subjects with Benign Prostatic Hyperplasia (BPH) who previously received an injection of NX-1207 in an earlier U.S. clinical trial of NX-1207.

Timeline

Start
2013-04
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject FEXAPOTIDE Protein / enzyme biologic 2.5 mg Other