drugset / Trial / NCT03850782

Evaluation of the Duration of Effect of Bimatoprost SR in Participants With Open-Angle Glaucoma or Ocular Hypertension

NCT03850782

Phase 3 Completed 515 enrolled AbbVie
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study evaluates the duration of intraocular pressure (IOP)-lowering effect and safety of as needed administrations of Bimatoprost sustained release (SR) in participants with open-angle glaucoma (OAG) or ocular hypertension (OHT) who are not adequately managed with topical IOP-lowering medication for reasons other than medication efficacy.

Timeline

Start
2019-02-28
Primary completion
2025-08-08
Completion
2025-08-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 10 ug Other