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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
Phase
Phase 3
Started
2026-02-17
Last updated
2026-03-30

Condition(s) studied

Glaucoma

Investigational drug(s) / intervention(s)

Gen 2 Travoprost Intracameral Implant →Timolol eye drops 0.5% →Sham Procedureplacebo eye drops

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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)

FacilityCityRegionStatus
Glaukos Investigative Site Dothan Alabama Recruiting
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