CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 130 enrolled
Drug / intervention
Bepreve (bepotastine besilate ophthalmic solution) 1.5% +2 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/NCT00586664
NCT00586664Phase 3Completed

Efficacy and Safety Study of Bepotastine Besilate Ophthalmic Solution in Allergic Conjunctivitis

Bausch & Lomb Incorporated·interventional·Posted Jan 4, 2008·Updated Feb 8, 2013

In Brief

A Phase 3 clinical trial evaluating Bepreve (bepotastine besilate ophthalmic solution) 1.5%, placebo comparator, and 1 other intervention for Allergic Conjunctivitis. Completed, enrolled 130 participants across 1 site.

Detailed Summary

Efficacy and safety study of bepotastine besilate ophthalmic solution in allergic conjunctivitis

Study Details

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

Timeline

Phase 3CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJan 4, 2008
Enrollment StartOct 1, 2007
Primary CompletionJun 1, 2008
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 18.5 years ago

Interventions

Bepreve (bepotastine besilate ophthalmic solution) 1.5%drug

sterile ophthalmic solution

placebo comparatordrug

sterile ophthalmic solution

Bepotastine Besilate Ophthalmic Solution 1.0%drug

sterile ophthalmic solution