Clinical Trials in the USA / NCT07495852
Recruiting
Phase 3
Trial to Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant
NCT07495852 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Glaucoma
Investigational drug(s) / intervention(s)
Gen 2 Travoprost Intracameral Implant: Travoprost
Timolol eye drops 0.5%: Timolol 0.5%
Sham Procedure: Sham implant administration
placebo eye drops: Artificial Tears
Study summary
Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant
Eligibility
Inclusion Criteria:
* Diagnosis of Ocular Hypertension or Open-Angle Glaucoma in the study eye
Exclusion Criteria:
* Prior incisional glaucoma surgery in the study eye
* Prior argon laser trabeculoplasty (ALT) in the study eye
* Prior minimally invasive glaucoma (MIGS) surgery in the study eye
Primary outcome measure(s)
- Intraocular pressure (IOP) — 3 months
Change from baseline in diurnal IOP in the study eye at 8am and 10am at each of Day 11, Week 6, and Month 3 visits
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Glaukos Investigative Site | Dothan | Alabama | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07495852 on ClinicalTrials.gov ↗ ← All trials in the USA