This trial is an open, national, multi-centre trial. The trial will be initiated after olive pollen season 2012 and subjects will receive treatment for 6 weeks. The aim of study is to assess the tolerability of the up-dosing phase of AVANZ Olive. The frequency of patients with adverse reactions will be the primary endpoint. Frequency of patients with systemic reactions according to EAACI classification, increase in IgG4 and in IgE and reduction in immediate skin reactivity.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
93
Immunotherapy Olea europaea
Hospital Universitario Reina Sofía
Córdoba, Córdoba, Spain
Frequency of patients with adverse reactions.
From date of inclusion until date of last visit documented, it's expected an average of 6 visits, assessed up to 6 weeks per subject.
Time frame: Participants will be followed for an expected average of 6 week.s
Frequency of patients with systemic reactions according to EAACI classification.
From date of inclusion until date of last visit documented, it's expected an average of 6 visits, assessed up to 6 weeks per subject.
Time frame: Participants will be followed for an expected average of 6 weeks.
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