drugset / Trial / NCT02537015

An Open-label Extension Study to Evaluate the Safety of the 13 mg Bimatoprost Ocular Insert

NCT02537015

Phase 2 Completed 81 enrolled ForSight Vision5, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This study evaluated the long-term (9-months) safety of the Bimatoprost Ocular Insert in participants with Glaucoma or Ocular Hypertension who completed study FSV5-004. All the participants received Bimatoprost Ocular Insert and wore it for approximately 3 months (12 weeks), then had that Insert removed and a new Insert placed for another 26 weeks (approximately 6 months).

Timeline

Start
2015-08-10
Primary completion
2016-08-11
Completion
2016-08-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 13 mg Other