A Multi-Center Randomized Study to Evaluate the Efficacy and Safety of an Investigational Lubricant Eye Drop

Study Identifier
AG9689-001
CT.gov Identifier
NCT00243711
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 sodium and Glycerin
    • Phase
    Phase 2/Phase 3
    Sex
    Female & Male
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Mild, Moderate, or Severe Dry Eye Symptoms and current eye drop use; * Reduced tear stability or tear production
    Exclusion Criteria:
    * NONE

    Protocol Summary

    The efficacy, safety and acceptability of an investigational lubricant eye drop in subjects with dry eye will be evaluated in comparison with currently-available lubricant eye drops.

    Study Locations

    Location
    Status
    Location
    Warrensburg, Missouri, United States
    Status
    Not applicable