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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 Oct 22, 2026, 10:51 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
Dec 2005 (Type not available)
Primary completion
Feb 2007 (Actual)
Completion
Feb 2007 (Actual)
Last update posted
Jan 20, 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 20, 2017 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00321477 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →