Assessment of Fluticasone Propionate on Ocular Allergy Symptoms

Completed · Phase 3 · Has a placebo group

Conditions studied: Allergic Rhinitis, Seasonal Allergic Rhinitis

In brief

This study is designed to investigate the efficacy of fluticasone propionate (FP) on ocular symptoms associated with allergic rhinitis (AR).

Key facts

Study ID

NCT01817790

Run by

GlaxoSmithKline

People needed

626

Starts

2012-12-01

Expected to finish

2013-02-01

Last updated by the study team

2014-04-03

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Participants with good general health (in the opinion of the investigator) with no clinically significant and relevant abnormalities of medical history
• Participants with diagnosis of seasonal allergic rhinitis
• A clinical history (written or verbal confirmation) of allergic rhinitis with the seasonal onset and offset of nasal and ocular allergy symptoms during each of the last 2 mountain cedar pollen allergy seasons.
• A positive skin test reaction to (at least) the relevant allergen, mountain cedar pollen, as determined by the skin pricks method performed within 12 months of Visit 1).
• Participants with allergic rhinitis symptom of at least moderate severity for randomization:
• An iTOSS of ≥ 4 and an iNCSS of ≥2 on the morning of randomization (Visit 3/Baseline).
• An averaged (rTOSS) of ≥ 4, and an averaged rNCSS of ≥2 for three of the five days during the placebo lead in
• Participant residing within a geographical environment where exposure to mountain cedar pollen is significant during the entire study period.
• Participant demonstrates understanding of the study and willingness to participate as evidenced by voluntary written informed consent/assent and has received a signed and dated copy of the informed consent/assent form. Children, ages 12 to 17 will be required to sign an assent form as part of the informed consent process.

You may not qualify if…

• Participants with known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds) or any of their stated ingredients.
• Participants with nasal disorders like:
• injury or surgery to their nose that the investigator believes would interfere with participation in the study.
• previously diagnosed with a severe physical obstruction of the nose (e.g., deviated septum) that could affect the deposition of double-blind intranasal study drug.
• Rhinitis medicamentosa
• Participants who have historical or current evidence of clinically significant uncontrolled disease like asthma, cardiac arrhythmias, hypertension, diabetes mellitus, ocular herpes, glaucoma, hepatic or renal disease, malignancy etc.
• Presence of or symptoms of an active bacterial or viral infection.
• Participants who have conjunctivitis caused by an infectious agent.
• Participants with current, single eye or bilateral cataracts or participants who had cataract surgery within/less than 3 months

Where it is running

• PPD Corporate Headquarters — Wilmington, North Carolina, United States

Full record on ClinicalTrials.gov

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