drugset / Trial / NCT00420082

A Randomized, Double-Blind, 4-way Crossover Study to Evaluate the Efficacy of Bilastine in the Vienna Challenge Chamber

NCT00420082

Phase 2 Completed 75 enrolled Faes Farma, S.A.
RandomizedCrossoverQuadruple-blindTreatment

Summary

This is a randomized, double blind, active and placebo controlled, 4 way crossover study in patients with seasonal allergic rhinitis. Patients will receive a single dose of bilastine 20 mg, Cetirizine 10 mg, Fexofenadine 120 mg, and placebo in the Vienna Challenge Chamber.

Timeline

Start
2006-10
Primary completion
Completion
2006-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Bilastine Small molecule 20 mg Oral
Comparator Cetirizine Other / unclassified 10 mg Oral
Comparator Fexofenadine Unknown 120 mg Oral