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A Phase 2 Prospective, Multicenter, Randomized, Double-masked, Controlled Study to Evaluate the Efficacy and Safety and Dose-response of the Bimatoprost Ocular Insert (2.2 mg, 13 mg) With and Without Concomitant Artificial Tears Compared to a Placebo Ocular Insert With and Without Concomitant Timolol (0.5%) Ophthalmic Solution in Patients With Open-angle Glaucoma or Ocular Hypertension

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Trial Profile

A Phase 2 Prospective, Multicenter, Randomized, Double-masked, Controlled Study to Evaluate the Efficacy and Safety and Dose-response of the Bimatoprost Ocular Insert (2.2 mg, 13 mg) With and Without Concomitant Artificial Tears Compared to a Placebo Ocular Insert With and Without Concomitant Timolol (0.5%) Ophthalmic Solution in Patients With Open-angle Glaucoma or Ocular Hypertension

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 05 Jun 2020

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At a glance

  • Drugs Bimatoprost (Primary) ; Timolol
  • Indications Ocular hypertension; Open-angle glaucoma
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors ForSight VISION5

    • Most Recent Events

    • 17 Nov 2015 Status changed from active, no longer recruiting to completed, according to a ForSight VISION5 media release.
    • 11 Jun 2015 According to a ForSight VISION5 company media release, company expecting top-line data from this trial in second half of 2015.
    • 11 Jun 2015 According to a ForSight VISION5 company media release, study enrolled 121 subjects at ten clinical sites in the USA in under nine weeks.
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