The purpose of this study is to determine whether it is safe to administer Ragweed-SPIRE to subjects suffering from both ragweed allergy and asthma.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
55
Intradermal injection
Kanata Allergy Services
Kanata, Ontario, Canada
Kingston General Hospital
Kingston, Ontario, Canada
Cheema Research Inc
Mississauga, Ontario, Canada
Ottawa Allergy Research Corp
Ottawa, Ontario, Canada
Number of subjects with adverse events as a measure of safety and tolerability
Time frame: Throughout subjects participation in the study, approximately 22 weeks
Number of subjects with asthma exacerbations as a measure of safety and tolerability
Time frame: Throughout subjects participation in the study, approximately 22 weeks
Evaluation of change in lung function as a measure of safety and tolerability
Time frame: Throughout subjects participation in the study, approximately 22 weeks
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Inflamax Research
Toronto, Ontario, Canada