Overview

An Open-Label, Long-Term Study With AL-4943A Ophthalmic Solution, 0.2% in Patients With Allergic Conjunctivitis

Status:
Completed
Trial end date:
2010-05-01
Target enrollment:
0
Participant gender:
All
Summary
The objective of this study is to assess safety and efficacy of long-term use of AL-4943A (Olopatadine Hydrochloride Ophthalmic Solution, 0.2%) in patients with allergic conjunctivitis.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Alcon Research
Treatments:
Olopatadine Hydrochloride
Ophthalmic Solutions
Pharmaceutical Solutions
Criteria
Inclusion Criteria:

- Subjects must provide written consent.

- Subjects must have a diagnosis of allergic conjunctivitis.

- Other protocol-defined inclusion criteria may apply.

Exclusion Criteria:

- Itching and/or hyperemia associated with diseases other than allergic conjunctivitis.

- Retinal detachment, diabetic retinopathy, or any progressive disease in posterior
segment of the eye.

- Known history of ocular infection.

- Contact lens wear during study.

- Pregnant, nursing.

- Participation in another clinical study within 30 days of Informed Consent.

- Other protocol-defined exclusion criteria may apply.