A Phase 1/2 Multicenter, Randomized, Controlled Dose-Finding Study to Evaluate the Safety and Ocular Hypotensive Efficacy of 3 Dose Levels of the VS101 Subconjunctival Latanoprost Insert for 3 Months in Subjects With Open-Angle Glaucoma or Ocular Hypertension

Trial Profile

A Phase 1/2 Multicenter, Randomized, Controlled Dose-Finding Study to Evaluate the Safety and Ocular Hypotensive Efficacy of 3 Dose Levels of the VS101 Subconjunctival Latanoprost Insert for 3 Months in Subjects With Open-Angle Glaucoma or Ocular Hypertension

Completed
Phase of Trial: Phase I/II

Latest Information Update: 16 Mar 2018

At a glance

  • Drugs Latanoprost (Primary)
  • Indications Glaucoma
  • Focus First in man; Therapeutic Use
  • Sponsors ViSci
  • Most Recent Events

    • 13 Mar 2018 Status changed from active, no longer recruiting to completed.
    • 24 Jul 2017 Results of Eye-D latanoprost inserts published in the BioLight Life Sciences Ltd media release.
    • 18 Apr 2017 Status changed from recruiting to active, no longer recruiting.
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