The purpose of this study is to determine whether Ragweed-SPIRE is safe and effective at reducing allergy symptoms in people who suffer from allergy to Ragweed pollen
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
280
Kanata Allergy Services
Kanata, Ontario, Canada
KGK Synergize Inc
London, Ontario, Canada
Inflamax Research
Mississauga, Ontario, Canada
Taunton Health Centre
Oshawa, Ontario, Canada
Change from Baseline in mean Total Rhinoconjunctivitis Symptom Score (TRSS)
Time frame: Between Baseline and approximately 25 weeks after randomisation
Change from baseline in mean Total Rhinoconjunctivitis Symptom Score (TRSS) - all timepoints
Time frame: Between Baseline and approximately 25 weeks after randomisation
Change from Baseline in mean Total Nasal Symptom Score (TNSS)
Time frame: Aproximately 25 weeks after randomisation
Change from Baseline in mean Total Non Nasal Symptom Scores (TNNSS)
Time frame: Approximately 25 weeks after randomisation
Number of Participants with Adverse Events as a Measure of Safety and tolerability
Time frame: Approximately 28 weeks
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Windsor Allergy Asthma Associates
Windsor, Ontario, Canada