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Completed Phase 3 Interventional

A Study To Evaluate The Efficacy And Safety Of A Once-Daily Investigational Nasal Spray In Adults And Adolescents With Perennial Allergic Rhinitis (PAR).

ClinicalTrials.gov ID: NCT00103454

Public ClinicalTrials.gov record NCT00103454. 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 3, 2026, 5:01 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

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Study to Evaluate the Efficacy and Safety of Once-Daily, Intranasal Administration of GW685698X Aqueous Nasal Spray 100mcg for 4 Weeks in Adult and Adolescent Subjects (12 Years of Age and Older) With Perennial Allergic Rhinitis (PAR)

Brief summary

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

The primary objective of this study is to compare the efficacy and safety of GW685698X 100mcg once daily (QD) aqueous nasal spray with vehicle placebo nasal spray in adult and adolescent subjects (12 years of age and older) with perennial allergic rhinitis (PAR).

Study identification

NCT ID
NCT00103454
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
288 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
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 31, 2004
Primary completion
Apr 30, 2005
Completion
Apr 30, 2005
Last update posted
Sep 18, 2016

2005

United States locations

U.S. sites
43
U.S. states
24
U.S. cities
40
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Los Angeles California 90025
GSK Investigational Site Mission Viejo California 92691
GSK Investigational Site Orange California 92868
GSK Investigational Site San Diego California 92120
GSK Investigational Site San Diego California 92123
GSK Investigational Site Colorado Springs Colorado 80907
GSK Investigational Site Miami Florida 33173
GSK Investigational Site Miami Florida 33176
GSK Investigational Site Tallahassee Florida 32308
GSK Investigational Site Tampa Florida 33613
GSK Investigational Site Vero Beach Florida 32960
GSK Investigational Site Lawrenceville Georgia 30045
GSK Investigational Site Lilburn Georgia 30047
GSK Investigational Site South Bend Indiana 46617
GSK Investigational Site Metairie Louisiana 70006
GSK Investigational Site Portland Maine 04102
GSK Investigational Site Baltimore Maryland 21236
GSK Investigational Site Rockville Maryland 20850
GSK Investigational Site North Andover Massachusetts 01845
GSK Investigational Site North Dartmouth Massachusetts 02747
GSK Investigational Site Springfield Massachusetts 01107
GSK Investigational Site St Louis Missouri 63104
GSK Investigational Site St Louis Missouri 63141
GSK Investigational Site Lincoln Nebraska 68505
GSK Investigational Site Omaha Nebraska 68130
GSK Investigational Site Ocean City New Jersey 07712
GSK Investigational Site Summit New Jersey 07091
GSK Investigational Site Raleigh North Carolina 27607
GSK Investigational Site Canton Ohio 44718
GSK Investigational Site Cincinnati Ohio 45231
GSK Investigational Site Oklahoma City Oklahoma 73104
GSK Investigational Site Eugene Oregon 97401
GSK Investigational Site Lake Oswego Oregon 97035
GSK Investigational Site Medford Oregon 97504
GSK Investigational Site Providence Rhode Island 02906
GSK Investigational Site Orangeburg South Carolina 29118
GSK Investigational Site Nashville Tennessee 37203-1424
GSK Investigational Site Austin Texas 78731
GSK Investigational Site New Braunfels Texas 78130
GSK Investigational Site Murray Utah 84107
GSK Investigational Site South Burlington Vermont 05403
GSK Investigational Site West Allis Wisconsin 53227

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00103454, 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 Sep 18, 2016 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00103454 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →