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A Randomized, Contralateral Study To Evaluate Corneal Endothelial Cell Density Changes In Healthy Subjects, When Administered 0.6% ISV-403 Three Times Daily For Five Days.

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Trial Profile

A Randomized, Contralateral Study To Evaluate Corneal Endothelial Cell Density Changes In Healthy Subjects, When Administered 0.6% ISV-403 Three Times Daily For Five Days.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 20 Feb 2013

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At a glance

  • Drugs Besifloxacin (Primary)
  • Indications Bacterial infections; Conjunctivitis; Ophthalmic infections
  • Focus Pharmacodynamics
  • Sponsors Bausch & Lomb

    • Most Recent Events

    • 13 May 2010 New trial record

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