drugset / Trial / NCT02121613

PERmixon® in LUTS Evaluation Study (PERLES)

NCT02121613

Phase 4 Completed 833 enrolled Pierre Fabre Laboratories
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The aim of this study is to support the efficacy of Permixon 160 mg b.i.d. in treating subjects with symptomatic Benign Prostatic Hyperplasia (BPH), compared to placebo, using Tamsulosine LP 0.4 mg as a reference treatment.

Timeline

Start
2014-04
Primary completion
2016-06
Completion
2016-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Permixon Unknown 160 mg Oral
Subject Tamsulosin Other / unclassified 0.4 mg Oral