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Clinical Trial Summary

The aim of this clinical phase I single centre, randomized, double-blind, placebo-controlled study with open comparator is to investigate tolerability and safety as well as the immunological effects of BM41 in comparison to placebo (double blind) and to a standard subcutaneous immunotherapy Alutard SQ (open) in birch allergic patients.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT04912076
Study type Interventional
Source Odense University Hospital
Contact
Status Completed
Phase Phase 1
Start date September 17, 2018
Completion date March 22, 2019

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