RecruitingPhase 2Phase 3NCT07075718

Phase 2/Phase 3 Trial to Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant


Sponsor

Glaukos Corporation

Enrollment

610 participants

Start Date

Jun 12, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a second-generation version of a small eye implant that slowly releases a glaucoma medication (travoprost) to lower eye pressure over time, offering a potential alternative to daily eye drops. **You may be eligible if...** - You have been diagnosed with open-angle glaucoma or ocular hypertension (high eye pressure) in the study eye **You may NOT be eligible if...** - You have previously had incisional (cutting) glaucoma surgery in the study eye - You have had argon laser trabeculoplasty (ALT) — a specific laser procedure — in the study eye - You have had minimally invasive glaucoma surgery (MIGS) in the study eye Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGGen 2 Travoprost Intracameral Implant

travoprost

DRUGTimolol eye drops 0.5%

timolol 0.5%

PROCEDURESham Procedure

sham implant administration

OTHERPlacebo eye drops

artificial tears


Locations(3)

Glaukos Investigative Site

Grand Junction, Colorado, United States

Glaukos Investigative Site

Oklahoma City, Oklahoma, United States

Glaukos Clinical Site

El Paso, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07075718


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