Safety and Efficacy of ENV515 Travoprost Extended Release (XR) in Patients With Bilateral Ocular Hypertension or Primary Open Angle Glaucoma

• Status: Completed
• Trial end date: 2019-02-13
• Target enrollment: 0
• Participant gender: All

Summary

This is a multiple cohort study that will evaluate the safety and efficacy of ENV515 travoprost XR in patients with open-angle glaucoma or ocular hypertension.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Envisia Therapeutics
• Treatments: Maleic acid; Ophthalmic Solutions; Pharmaceutical Solutions; Timolol; Travoprost

Criteria

Inclusion Criteria:

• Diagnosis of either ocular hypertension or open angle glaucoma in both eyes.

• Are currently treated with topical PGA for ocular hypertension in both eyes.

• Patients who in the opinion of the Investigator: have an IOP in both eyes that is considered to be adequately controlled, can be safely withdrawn from IOP medications in both eyes during the washout period, and who are not considered to be at significant risk for disease progression throughout the trial.

Exclusion Criteria:

• Eye surgery (including cataract surgery) within the past 3 months.

• History of glaucoma related surgery.