A Study Of GW679769 Compared To Placebo In Women With Overactive Bladder

Status Completed

Clinical Trial Summary

This is a Phase IIa study to evaluate the efficacy, safety and tolerability of GW679769 vs placebo on symptoms of urgency with urge incontinence, frequency and nocturia associated with overactive bladder in women.

Clinical Trial Description

A Twelve-Week Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Forced Titration, Proof of Concept Study to Assess the Efficacy, Safety and Tolerability as well as the Pharmacokinetic Profile of 60 mg and 120 mg of GW679769 administered once daily vs Placebo in Women with Overactive Bladder ;

Study Design

Related Conditions & MeSH terms

Enuresis
Incontinence, Urinary and Urinary Bladder, Overactive
Overactive Bladder
Urinary Bladder, Overactive
Urinary Incontinence

Clinical Trial Details

NCT number	NCT00321477
Study type	Interventional
Source	GlaxoSmithKline
Contact
Status	Completed
Phase	Phase 2
Start date	December 2005
Completion date	February 2007

View Details

See also
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