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Primary Open Angle Glaucoma Treatment Trial

Study Title

A Dose-Escalation Study Designed to Evaluate the Tolerability, Safety, Pharmacokinetics (PK), and Efficacy of Chronic Topical Ocular Application of INO-8875 in Adults With Ocular Hypertension or Primary Open-Angle Glaucoma

Enrollment Status

This study is currently recruiting participants.

Purpose

The purpose of this study is to evaluate how tolerable, safe, and effective it is to give INO-8875 eye drops to adults with glaucoma or ocular hypertension.

Eligibility

Ages Eligible for Study: 18 Years to 75 Years

Genders Eligible for Study: Both

Inclusion Criteria

• Subjects with the diagnosis of ocular hypertension (OHT) or primary open-angle glaucoma (POAG).
• Aged 18 to 75 years.
• Mean intraocular pressure (IOP) of ≥24 and ≤34 mm Hg.

Contact Information

Dr. Paul Sidoti, Glaucoma Specialist
Katy Tai, Research Manager
ktai@nyee.edu or 212-979-4251

 

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