This study will compare the effectiveness of QAV680 against placebo in treating the symptoms of seasonal allergic rhinitis in an Environmental Exposure Chamber.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
44
Novartis Investigator Site
Toronto, Canada
Total Nasal Symptom Score (TNSS) over the last 2 hours of exposure in the EEC Percentage nasal lavage eosinophil count post EEC
Time frame: TNSS: 6-8h during EEC exposure on Day 10
Measure of nasal cytokines (ECP, IL-5, IL-13, PGD2, Eotaxin)
Time frame: After 8h exposure in EEC
Absolute eosinophil count from nasal lavage collected
Time frame: During exposure in EEC
Nasal airway patency assessed by acoustic rhinometry during exposure in the EEC
Time frame: During exposure in EEC
Total Ocular Symptom Score measured during exposure in the EEC
Time frame: During exposure in EEC
Assess pharmacokinetics of plasma QAV680 in patients with seasonal allergic rhinitis
Time frame: Through out study
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