drugset / Trial / NCT01861522

The Confirmatory Study of TAU-284 in Pediatric Patients With Perennial Allergic Rhinitis

NCT01861522 ↗

Phase 3 Completed 473 enrolled Tanabe Pharma Corporation
RandomizedParallel-groupTriple-blindTreatment

Summary

The objectives of this study are: to confirm the superiority of TAU-284 over placebo after two weeks of administration to pediatric patients with perennial allergic rhinitis and to investigate safety of TAU-284.

Timeline

Start
2013-04
Primary completion
2013-12
Completion
2013-12

Outcome

Met primary endpoint

paper Bepotastine besilate was superior to placebo in terms of total nasal symptom scores, with improved overall nasal symptoms of PAR compared with baseline values. PMID 26364765 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bepotastine Small molecule 10 mg Oral