Evaluating Injection With the Use of Brimonidine Tartrate Ophthalmic 0.025% on Patients Using Netarsudil 0.02%/Latanoprost 0.005% to Treat Glaucoma

Recruiting now · Phase 4

Conditions studied: Glaucoma

In brief

To evaluate the effect of brimonidine tartrate 0.025% on conjunctival hyperemia in patients treated with netarsudil 0.02%/latanoprost 0.005% mono-therapy for intraocular pressure lowering.

Key facts

Study ID

NCT07209410

Run by

Insight Eyecare Specialties, Inc. dba Vision Source Eyecare,

People needed

35

Starts

2025-11-01

Expected to finish

2027-06-01

Last updated by the study team

2025-11-18

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 1. Adult patients 18-65 years old diagnosed with open-angle glaucoma or ocular hypertension.
• Currently on netarsudil 0.02%/latanoprost 0.005% monotherapy for a minimum of 2-6 weeks.
• Able to move from current topical glaucoma treatment to netarsudil 0.02%/latanoprost 0.005% for a minimum of 4 weeks or longer based on FDA recommended washout per drug classification prior to Visit 3.
• Experience conjunctival redness as graded on the Efron scale of at least grade 2 after minimum of 4 weeks on netarsudil 0.02%/latanoprost 0.005% mono-therapy or longer based on recommended washout per drug classification 4. Have a best corrected Visual Acuity by Snellen chart of 20/30 or better in study eye.
• Are willing and able to self-administer or have an able person available to assist with administration of study drug.
• Willing and able to comply with study procedures and attend follow-up visits.

You may not qualify if…

• Allergy or hypersensitivity to brimonidine or other components of brimonidine tartrate 0.025% or netarsudil 0.02%/latanoprost 0.005%.
• Use of any other topical ocular medications.
• Active ocular infection, inflammation unrelated to glaucoma therapy, uveitis, iritis or congenital aphakia.
• Have pterygium/pinguecula, chemosis, episcleritis, scleritis (or any condition that may affect hyperemia grading) in the opinion of the investigator
• Have moderate or severe dry eyes.
• Pregnant, plan to become pregnant or breastfeeding.
• Concurrent or past use in the last 90 days of vasoconstrictive ocular drops other than brimondine 0.025%
• Have undergone previous incision IOP lowering surgeries.
• Have undergone previous laser surgery for glaucoma (selective laser trabeculoplasty (SLT) or argon laser trabeculoplasty (ALT)), or microinvasive glaucoma surgery (MIGS) with 6 months of screening.
• Have had intraocular or per-ocular surgery within the past 3 months.
• Advanced glaucoma or c/d ratio greater than 0.8. Are non-responsive to topical treatment with netarsudil 0.02%/latanoprost 0.005%.
• In the judgement of the investigator, have previous or currently active clinically significant systemic or ocular disease in either eye that could affect study outcomes.

Where it is running

• Vision Source — Kansas City, Missouri, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.