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A Randomized, Multi-Center, Parallel-Group, Safety and Efficacy Study of Lotemax Gel 0.5% and Restasis 0.05% for 12 Weeks in Subjects With Mild or Moderate Keratoconjunctivitis Sicca (Dry Eye Disease; DED)

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A Randomized, Multi-Center, Parallel-Group, Safety and Efficacy Study of Lotemax Gel 0.5% and Restasis 0.05% for 12 Weeks in Subjects With Mild or Moderate Keratoconjunctivitis Sicca (Dry Eye Disease; DED)

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 14 Jan 2020

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At a glance

  • Drugs Loteprednol etabonate (Primary) ; Allantoin; Ciclosporin
  • Indications Keratoconjunctivitis sicca
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Bausch & Lomb

    • Most Recent Events

    • 20 Aug 2014 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov record.
    • 03 Dec 2013 New trial record

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