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Study identifier: NCT02129673 Synced from ClinicalTrials.gov · August 10, 2026
● Study status: Completed

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

Condition: Open Angle Glaucoma · Ocular Hypertension  ·  Sponsor: ViSci Ltd.

PhasePhase 1/Phase 2
Planned participants77
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersNoCheck eligibility criteria ↓
WhereBellevue, Washington, United States
For sponsors, CROs & site teams
Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.Open the site landscape →

About this study

Slow release formulation of latanoprost is compared for safety and pressure-lowering efficacy with topically administration of commercially available latanoprost in patient with glaucoma and ocular hypertension

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

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Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Age \> 18 * Open angle glaucoma or Ocular Hypertension Exclusion Criteria: * uncontrolled medical conditions * wearing of contact lenses

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Speciality Eyecare CentreBellevue, Washington, United States

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Bellevue

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