Safety and Tolerability of Artificial Tears in Dry Eye Subjects

Study Identifier
AG9965-001
CT.gov Identifier
NCT00932477
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Study Details

Medical Condition
  • Dry Eye
    • Study Drug
  • Formulation 1: Carboxymethylcellulose Sodium, Glycerin and Polysorbate 80, based artificial tear
  • Formulation 2: Carboxymethylcellulose Sodium, Glycerin and Polysorbate 80, based artificial tear
  • Glycerin and Polysorbate 80 based artificial tear
    • Phase
    N/A
    Sex
    Female & Male
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Mild, moderate or severe symptoms of dry eye
    Exclusion Criteria:
    * Uncontrolled systemic disease * Contact lens wear * Participation in another clinical study

    Protocol Summary

    The safety and tolerability of two new artificial tears will be compared to a currently-available artificial tear in subjects with dry eye. Each subject will receive all three products in a randomly assigned order. The subject will use one product at a time for a duration of one week before switching to the next assigned product.

    Study Locations

    Location
    Status
    Location
    San Diego, California, United States
    Status
    Not applicable