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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT00321477

Public ClinicalTrials.gov record NCT00321477. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 5:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

NK1 Receptor Antagonist vs Placebo in the Treatment of Overactive Bladder Symptoms

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00321477
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
160 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2005
Primary completion
Jan 31, 2007
Completion
Jan 31, 2007
Last update posted
Jan 19, 2017

2005 – 2007

United States locations

U.S. sites
41
U.S. states
20
U.S. cities
39
Facility City State ZIP Site status
GSK Investigational Site Huntsville Alabama 35801
GSK Investigational Site Peoria Arizona 85381 - 4828
GSK Investigational Site Phoenix Arizona 85023
GSK Investigational Site La Mesa California 91942
GSK Investigational Site Modesto California 95350
GSK Investigational Site San Bernardino California 92404
GSK Investigational Site Torrance California 90506
GSK Investigational Site Aurora Colorado 80012
GSK Investigational Site Denver Colorado 80210
GSK Investigational Site Denver Colorado 80211
GSK Investigational Site Longmont Colorado 80501
GSK Investigational Site Waterbury Connecticut 06708
GSK Investigational Site Aventura Florida 33180
GSK Investigational Site Clearwater Florida 33761
GSK Investigational Site Fort Myers Florida 33916
GSK Investigational Site Miami Florida 33143
GSK Investigational Site Miami Florida 33156
GSK Investigational Site Ocala Florida 34474
GSK Investigational Site Pembroke Pines Florida 33024
GSK Investigational Site Sarasota Florida 34237
GSK Investigational Site Atlanta Georgia 30309
GSK Investigational Site Melrose Park Illinois 60160
GSK Investigational Site Indianapolis Indiana 46254
GSK Investigational Site Jeffersonville Indiana 47130
GSK Investigational Site Newburgh Indiana 47630
GSK Investigational Site Lexington Kentucky 40509
GSK Investigational Site Albany New York 12205
GSK Investigational Site Kingston New York 12401
GSK Investigational Site Poughkeepsie New York 12601
GSK Investigational Site Salisbury North Carolina 28144
GSK Investigational Site Winston-Salem North Carolina 27103
GSK Investigational Site Springfield Oregon 97477
GSK Investigational Site Bala-Cynwyd Pennsylvania 19004
GSK Investigational Site Lancaster Pennsylvania 17604
GSK Investigational Site Sellersville Pennsylvania 18960
GSK Investigational Site Providence Rhode Island 02906
GSK Investigational Site Simpsonville South Carolina 29681
GSK Investigational Site Nashville Tennessee 37232
GSK Investigational Site Dallas Texas 75234
GSK Investigational Site Richmond Virginia 23294
GSK Investigational Site Tacoma Washington 98405

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00321477, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 19, 2017 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00321477 live on ClinicalTrials.gov.

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