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
| Type | Name | Description |
|---|---|---|
| DRUG | Olopatadine HCl ophthalmic solution, 0.1% | |
| DRUG | Epinastine 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.