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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 Oct 19, 2026, 12:30 PM 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
Jan 2005 (Type not available)
Primary completion
May 2005 (Actual)
Completion
May 2005 (Actual)
Last update posted
Sep 19, 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 19, 2016 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00103454 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →