Clinical Trials Directory

Trials / Completed

CompletedNCT01109485

Clinical Evaluation of 0.1% Olopatadine Hydrochloride Ophthalmic Solution in Pediatric Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
7 Years – 15 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to further evaluate the safety of Olopatadine Ophthalmic Solution 0.1% in Japanese children with allergic conjunctivitis.

Conditions

Interventions

TypeNameDescription
DRUGOlopatadine hydrochloride ophthalmic solution 0.1%1-2 drops 4 times per day

Timeline

Start date
2010-03-01
Primary completion
2011-07-01
Completion
2011-07-01
First posted
2010-04-23
Last updated
2015-05-12

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT01109485. Inclusion in this directory is not an endorsement.