Safety and Efficacy of an Artificial Tear for the Treatment of Dry Eye

Study Identifier
AG9818-002
CT.gov Identifier
NCT00514852
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
  • Carboxymethylcellulose and Glycerin based artificial tear
  • Carboxymethylcellulose
    • 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 * Use of systemic medications affecting dry eye * Pregnancy or planning a pregnancy * Contact lens wear

    Protocol Summary

    The efficacy, safety and acceptability of a new artificial tear in subjects with dry eye will be compared to a currently-available artificial tear

    Study Locations

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