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S.C. Immunotherapy With BM41 in Patients With Allergic Rhino-conjunctivitis Caused by Birch Pollen — BM41  

Allergic Rhinoconjunctivitis Clinical Trial

Official title:
A Randomized, DBPC Study to Determine the Safety, Tolerability and Immunological Effects of BM41 Compared to Placebo and to Treatment With Standard s.c. Immunotherapy in Patients Allergic to Birch Pollen

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

Please see original article. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
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
View Details
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