At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Safety and Efficacy of AGN-210961 Ophthalmic Solution Compared With Bimatoprost Ophthalmic Solution in Patients With Glaucoma or Ocular Hypertension
In Brief
A Phase 2 clinical trial evaluating AGN-210961 Formulation 1, AGN-210961 Formulation 2, and 6 other interventions for Ocular Hypertension and Primary Open-Angle Glaucoma. Completed, enrolled 163 participants across 1 site.
Detailed Summary
This study has 2 parts. Part 1 will evaluate the safety and IOP effects of 6 formulations of AGN-210961 ophthalmic solution in the study eye and bimatoprost ophthalmic solution 0.03% in the fellow eye for 7 consecutive days. Part 2 will evaluate the safety and IOP effects of a formulation (to be selected from part 1) of AGN-210961 in both eyes compared to bimatoprost ophthalmic solution 0.03% for 4 weeks.
Study Details
Timeline
Interventions
AGN-210961 Formulation 1 in one eye once daily for 7 days.
AGN-210961 Formulation 2 in one eye once daily for 7 days.
AGN-210961 Formulation 3 in one eye once daily for 7 days.
AGN-210961 Formulation 4 in one eye once daily for 7 days.
AGN-210961 Formulation 5 in one eye once daily for 7 days.
AGN-210961 Formulation 6 in one eye once daily for 7 days.
AGN-210961 Formulation 7 in both eyes once daily for 4 weeks.
bimatoprost ophthalmic solution 0.03% (LUMIGAN®) in both eyes once daily for 4 weeks.