A Study of GW685698X for the Treatment Of Perennial Allergic Rhinitis in Adolescents and Adults
Completed · Phase 3
Conditions studied: Rhinitis, Allergic, Perennial
In brief
The purpose of this study is to assess the effect of an aqueous nasal spray investigational compound compared to placebo on the hypothalamic pituitary adrenocortical (HPA) axis system in adolescents and adults 12 to 65 years of age with perennial allergic rhinitis. This study can last up to 6 weeks and you will come to the clinic up to 7 times. Clinic visits include physical examinations, vital sign assessments, clinical laboratory assessments, ECGs and allergy skin testing. You will need to complete a daily diary card and spend the night in the clinic on 2 occasions to collect urine and blood samples over 24 hour periods.
Key facts
- Study ID
- NCT00116818
- Run by
- GlaxoSmithKline
- People needed
- 90
- Starts
- 2005-01-01
- Expected to finish
- 2005-05-01
- Last updated by the study team
- 2016-09-15
Who can join
Age: 12 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis and history of perennial allergic rhinitis.
- Must be willing to stay overnight in the clinic at the beginning and end of the study for the collection of urine and blood samples over 24 hours.
- Must comply with all study procedures and be literate.
You may not qualify if…
- Use of tobacco products.
- Work a rotating shift.
- Significant concurrent medical conditions.
- Certain medications such as corticosteroids and allergy medications.
Where it is running
- GSK Investigational Site — San Antonio, Texas, United States
- GSK Investigational Site — Mississauga, Ontario, Canada
Full record on ClinicalTrials.gov
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