The primary objective of the trial is to evaluate the dose-response relationship with regards to change in immunological parameters and safety for SLITone ULTRA house dust mite mix in adult subjects with moderate to severe HDM allergic rhinitis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
219
Proffesor Alain Didier
Toulouse, France
Change from baseline in IgE-blocking factor after 6 months of treatment
Time frame: 6 months
Number of subjects with treatment related adverse events
Time frame: 6 months
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