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)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07075718
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