A Randomized Double-masked 14-day Study to Compare the Ocular Safety, Tolerability, and Efficacy of Differing Dosing Regimens of ISV-303 (0.075% Bromfenac in DuraSite [Rm]) to Vehicle and Xibrom [Rm] in Post Cataract Surgery Volunteers.

Trial Profile

A Randomized Double-masked 14-day Study to Compare the Ocular Safety, Tolerability, and Efficacy of Differing Dosing Regimens of ISV-303 (0.075% Bromfenac in DuraSite [Rm]) to Vehicle and Xibrom [Rm] in Post Cataract Surgery Volunteers.

Completed
Phase of Trial: Phase I/II

Latest Information Update: 01 Dec 2017

At a glance

  • Drugs Bromfenac (Primary)
  • Indications Ocular inflammation; Ocular pain; Postoperative pain
  • Focus Therapeutic Use
  • Sponsors InSite Vision
  • Most Recent Events

    • 01 Dec 2017 Results (n=85) of comparative subgroup (QD group and BID group) analysis published in the Ophthalmology and Therapy
    • 23 Mar 2011 NCT reports actual end date as (1 Jan 2011).
    • 21 Mar 2011 Secondary endpoint 'Patient-assessment-of-pain' has been met.
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