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Study to Evaluate Safety, Tolerability and Explorative Efficacy of DM-101PX in Birch Pollen Allergic Participants

Birch Pollen Allergy Clinical Trial

Official title:
A Phase I Dose Escalation Trial to Investigate the Safety, Tolerability, and Explorative Efficacy, Following Environmental Allergen Exposure in a Chamber, of DM-101PX in Participants With Birch Pollen Allergy

Clinical Trial Summary

Randomized, double-blind placebo-controlled phase I trial with the primary aim to investigate safety and tolerability of three ascending dosing schemes of DM-101-PX in birch pollen allergic adults. As an explorative objective, the trial will also investigate the effect of DM-101PX on the allergic symptoms following birch pollen allergen exposure in a chamber. Expanded access to the study treatment is not available.

Clinical Trial Description

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

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06037148
Study type Interventional
Source Desentum Oy
Contact
Status Completed
Phase Phase 1
Start date September 7, 2023
Completion date March 6, 2024
View Details
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