Clinical Trials Directory

Trials / Completed

CompletedNCT02251613

Effectiveness of Olopatadine HCl Ophthalmic Solution for the Treatment of Allergic Conjunctivitis in Japan

Effectiveness of Olopatadine HCl Ophthalmic Solution, 0.1% Compared to Epinastine HCl Ophthalmic Solution, 0.05% in the Treatment of Allergic Conjunctivitis to Japanese Cedar Pollen

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effectiveness and safety of Olopatadine Hydrochloride (HCl) ophthalmic solution 0.1% versus Epinastine HCl ophthalmic solution, 0.05% in a population of healthy, adult Japanese patients (20 years of age or older) with a history of allergic conjunctivitis to Japanese Cedar Pollen. Patients will be randomly assigned to receive Olopatadine HCl ophthalmic solution, 0.1% in one eye and Epinastine HCl ophthalmic solution, 0.05% in the fellow eye, after which a conjunctival allergy challenge (CAC) with Japanese cedar pollen will be performed.

Conditions

Interventions

TypeNameDescription
DRUGOlopatadine HCl ophthalmic solution, 0.1%
DRUGEpinastine HCl ophthalmic solution, 0.05%

Timeline

Start date
2013-12-01
Primary completion
2014-01-01
Completion
2014-01-01
First posted
2014-09-29
Last updated
2015-10-07
Results posted
2015-02-09

Source: ClinicalTrials.gov record NCT02251613. Inclusion in this directory is not an endorsement.

Effectiveness of Olopatadine HCl Ophthalmic Solution for the Treatment of Allergic Conjunctivitis in Japan (NCT02251613) · Clinical Trials Directory