CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 89 enrolled
Drug / intervention
bepotastine besilate nasal product - low dose +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01222299
NCT01222299Phase 2Completed

Safety, Pharmacokinetics, and Efficacy of Bepotastine Besilate Nasal Product After Ragweed Pollen Exposure in an Environmental Chamber

Bausch & Lomb Incorporated·interventional·Posted Oct 18, 2010·Updated Oct 5, 2020

In Brief

A Phase 2 clinical trial evaluating bepotastine besilate nasal product - low dose, bepotastine besilate nasal product - medium dose, and 2 other interventions for Seasonal Allergic Rhinitis. Completed, enrolled 89 participants across 1 site.

Detailed Summary

The purpose of this study is to examine the safety and efficacy of bepotastine besilate nasal product in seasonal allergic rhinitis patients.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedOct 18, 2010
Enrollment StartMay 1, 2010
Primary CompletionAug 1, 2010
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 15.7 years ago

Interventions

bepotastine besilate nasal product - low dosedrug

sterile nasal product

bepotastine besilate nasal product - medium dosedrug

sterile nasal product

bepotastine besilate nasal product - high dosedrug

sterile nasal product

placebo comparator nasal productdrug

sterile nasal product