Condition: Allergic Conjunctivitis · Sponsor: Alcon Research
The purpose of this study is to assess the ocular comfort and safety of olopatadine hydrochloride opthalmic solution. 0.7%.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
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Inclusion Criteria: * Able to be dosed in both eyes, to follow instructions, and willing and able to attend required study visits. * Negative urine pregnancy test if female of childbearing potential and use adequate birth control throughout the study period. * Other protocol-defined inclusion criteria may apply. Exclusion Criteria: * History or clinical evidence of ocular herpes simplex or ocular herpes zoster infectious disease. * History of any clinically significant external ocular disease within 30 days of the start of the study. * Presence of active blepharitis, active meibomian gland dysfunction, active rosacea affecting the ocular surface/lid margin, active or chronic follicular conjunctivitis, preauricular adenopathy, or any other ocular or periocular abnormality that may affect the study outcomes. * Other protocol-defined exclusion criteria may apply.
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| Locations not yet listed on the registry record. |
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