The purpose of this study is to determine the safety and tolerability of several doses of ragweed pollen allergen extract administered as sublingual tablets in subjects with allergic rhinitis to ragweed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
60
administered once a day over 10 days
DRC Drug Research Center
Balatonfüred, Hungary
Safety, tolerability as indicated by adverse events and safety laboratory evaluation assessed every day over 2 weeks
Time frame: 2 weeks
Immunological markers (IgE and IgG4)
Time frame: 2 weeks
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