drugset / Trial / NCT06126952

Azelastine Allergen Chamber - Onset of Action Study

NCT06126952

Phase 2 Completed 84 enrolled MEDA Pharma GmbH & Co. KG
RandomizedCrossoverDouble-blindTreatment

Summary

This study is to assess the Onset of Action and Efficacy of azelastine hydrochloride 0.15% in treating the nasal symptoms of seasonal allergic rhinitis (SAR) induced by an allergen challenge in an Environmental Exposure Unit (EEU) followed by a single dose and a 3-day treatment at home.

Timeline

Start
2023-10-30
Primary completion
2024-02-23
Completion
2024-03-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Azelastine Small molecule 1644 ug Intranasal
Subject Mometasone furoate Other / unclassified 200 ug Intranasal
Subject Olopatadine Other / unclassified 4800 ug Intranasal