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NCT02129673 — "A Phase 1/2 Multicenter, Randomized, Study to Evaluate the Safety and Efficacy of VS101 Subconjunctival Latanoprost Insert in Subjects With Open-Angle Glaucoma or Ocular Hypertension" trial site landscape

Public-registry site landscape for NCT02129673, “A Phase 1/2 Multicenter, Randomized, Study to Evaluate the Safety and Efficacy of VS101 Subconjunctival Latanoprost Insert in Subjects With Open-Angle Glaucoma or Ocular Hypertension”, a Open Angle Glaucoma study sponsored by ViSci Ltd.. All data below is from public sources; Eichor is not affiliated with the sponsor.

TrialNCT02129673 (registry record)
Study titleA Phase 1/2 Multicenter, Randomized, Study to Evaluate the Safety and Efficacy of VS101 Subconjunctival Latanoprost Insert in Subjects With Open-Angle Glaucoma or Ocular Hypertension
Official titleA 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
SponsorViSci Ltd.
Condition(s)Open Angle Glaucoma; Ocular Hypertension
PhasePHASE1 / PHASE2
Listed sites1
Site countriesUnited States

Patient-friendly overview of this study: eichor.com/study/NCT02129673.

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