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Study to Evaluate Safety and Tolerability of sc Immunotherapy With DM-101 in Adults With Birch Pollen Allergy

Birch Pollen Allergy Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled, Dose Escalation Study to Evaluate the Safety and Tolerability of Subcutaneous Immunotherapy With DM-101 in Adults With Birch Pollen Allergy

Clinical Trial Summary

Randomized, double-blind placebo-controlled phase I study to investigate the safety and tolerability of ascending doses of DM-101 in adult subjects with birch pollen allergy.

Clinical Trial Description

The study will be carried out in a single study site located in Finland. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04266028
Study type Interventional
Source Desentum Oy
Contact
Status Completed
Phase Phase 1
Start date February 11, 2020
Completion date May 31, 2021
View Details
See also
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