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Clinical Trial Summary

This study is a proof-of-concept study to demonstrate if a daily dose of a 2-days pre-treatment of Fexofenadine 180mg is effective in alleviating the AR symptoms and to assess the additional benefit to the patient in terms of preventing Allergic Rhinitis (AR) symptoms. The total study duration per participant is expected at least 4 months, depending on the timing of the screening visit. 5 visits are planned, screening, confirmation inclusion challenge, randomization visit, challenge and end of study visit.


Clinical Trial Description

The end of the study is defined as the date of the last visit of the last participant in the study. A participant is considered to have completed the study if he/she has completed all visits of the study including Visit 5 (Day 5). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05692154
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 3
Start date January 23, 2023
Completion date March 14, 2023

See also
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