Clinical Trials Logo

Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Allergic Rhinitis Due to Olea Europaea Pollen

NCT number NCT01674595
Study type Interventional
Source ALK-Abelló A/S
Contact
Status Completed
Phase Phase 2/Phase 3
Start date September 2012
Completion date April 2013