Trial intelligence / Profile preview

Bioequivalence Study of Bilastine 20 mg Oral Dispersible Tablets in Healthy Adults

NCT07042828Phase 1Completed

Sponsor
Humanis
Start
Apr 2025
Primary completion
Jun 2025
Modality
Small Molecules
Countries
1
01

Overview

Phase 1, randomised, open-label trial of bilastine in allergic rhinoconjunctivitis (ARC) and urticaria (2 arms), sponsored by Humanis. Primary endpoints: Peak Plasma Concentration at 24 hours and Area Under the Curve from time zero to time of last measurable concentration at 24 hours. Started Apr 2025; status: completed.

02

Drugs

bilastine
03

Conditions

allergic rhinoconjunctivitis (ARC)urticaria

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