drugset / Trial / NCT04285580

A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of Bimatoprost SR in Patients With Open-Angle Glaucoma or Ocular Hypertension

NCT04285580

Phase 3 Completed 37 enrolled AbbVie
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the 24-hour intraocular pressure lowering effect and safety after a single administration of Bimatoprost SR in patients with Open-Angle Glaucoma or Ocular Hypertension

Timeline

Start
2020-06-11
Primary completion
2022-05-14
Completion
2022-05-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 10 ug Intravitreal
Subject Bimatoprost Other / unclassified 0.01 % Topical