Rhinoconjunctivitis Clinical Trial
Official title:
ZU-SkinSIT-001 Single Center Phase I/IIa, Placebo Controlled, Randomized, Double Blind Study to Assess the Clinical Efficacy and Safety of a Novel Method of Specific Allergen Immunotherapy in Grass Pollen Allergic Subjects by Epicutanous Allergen Administration
Primary Objective Comparison of the inhibition of the allergic response assessed by nasal
provocation test after epicutanous pollen allergen administration and placebo epicutaneous
administration.
Secondary Objectives Comparison of the efficacy of the placebo with that of the epicutanous
pollen allergen administration evaluated by visual analog symptom scales (nasal itching,
sneezing, rhinorrhea, conjunctival redness, and lacrimation, lung symptoms ), Comparison of
the inhibition of the allergic response assessed by skin prick test after epicutanous pollen
allergen administration and placebo epicutaneous administration.
- Trial with medicinal product
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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