Trial Profile

A 12-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Dose-Finding Study To Evaluate The Efficacy, Tolerability And Safety Of Fesoterodine In Comparison To Placebo In Patients With Overactive Bladder.

Status: Completed

Phase of Trial: Phase II

Latest Information Update: 09 Apr 2014

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At a glance

08 Feb 2014 Results from posthoc analysis of secondary endpoint (measures of nocturia) published in the Urology.
03 Jul 2009 Tria locations added as reported by ClinicalTrials.gov.
09 Feb 2009 Status changed from recruiting to completed as reported by ClinicalTrials.gov.

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