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Clinical Trial Summary

The purpose of this study is to assess the tolerability of AVANZ.


Clinical Trial Description

To assess the tolerability of the up-dosing phase of AVANZ Phleum pratense. The frequency of patients with adverse reactions will be the study primary endpoint. ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01454531
Study type Interventional
Source ALK-Abelló A/S
Contact
Status Completed
Phase Phase 2/Phase 3
Start date June 2011
Completion date April 2012

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