drugset / Trial / NCT02143843

An Open-Label Extension Study to Evaluate the Safety of the ForSight VISION5 Product

NCT02143843

Phase 2 Completed 75 enrolled ForSight Vision5, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This study evaluates the long-term (13-months) safety of the Bimatoprost Ocular Insert in participants with Glaucoma or Ocular Hypertension who completed study FSV5-002. All participants received Bimatoprost Ocular Insert and wore it for approximately 7 months, then had the Insert removed and a new insert placed for another 6 months.

Timeline

Start
2014-06-05
Primary completion
2015-12-31
Completion
2016-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 13 mg