Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subjects With Dry Eye Disease

Study Identifier
10146X-001
CT.gov Identifier
NCT01459588
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 Based Eye Drop Formulation A
  • Carboxymethylcellulose Based Eye Drop Formulation B
  • Carboxymethylcellulose Based Preservative-Free Lubricant Eye Drops
  • Carboxymethylcellulose Based Lubricant Eye Drops
    • Phase
    Phase 3
    Sex
    Female & Male
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Dry eyes * Current use of eye drops for dry eye at least twice daily, on average for at least 3 months
    Exclusion Criteria:
    * Cataract, laser-assisted in situ keratomileusis (LASIK), or photorefractive keratectomy (PRK) surgery in the last 12 months * Need to wear contact lenses during the study, or has worn contact lenses in the last 6 months * Active ocular allergy

    Protocol Summary

    This study will evaluate the safety, efficacy, and acceptability of an eye drop formulation in subjects with dry eye disease.

    Study Locations

    Location
    Status
    Location
    Petaluma, California, United States
    Status
    Not applicable