Clinical trial Recruiting at 3 sites Phase 2 Interventional Ages 18 and up

Second-generation travoprost intracameral implant for open-angle glaucoma and ocular hypertension

Official title: Phase 2 Trial to Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant

Run by Glaukos Corporation · NCT07075718 · Data updated 2026-11-12

This trial will test whether a second-generation travoprost implant placed inside the eye lowers eye pressure better than timolol eye drops in people with open-angle glaucoma or ocular hypertension.

Quick facts

PhasePhase 2
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment110 (estimated)
SponsorGlaukos Corporation
Industry-sponsored
Locations3 sites (Grand Junction, Colorado and 2 other locations)
StatusRecruiting
StartedJune 12, 2025
Main results expectedMarch 2028
Study endsMarch 2032
Registry record updatedSeptember 17, 2026
Trial IDNCT07075718 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with open-angle glaucoma or ocular hypertension who have not had prior incisional glaucoma surgery, ALT, or MIGS in the study eye are appropriate candidates for this protocol.

Probably not a fit

Patients with prior incisional glaucoma surgery, prior ALT, or prior MIGS in the study eye are excluded and would not be expected to benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized Phase 2/3 trial compares a second-generation travoprost intracameral implant to timolol 0.5% eye drops given twice daily in adults with open-angle glaucoma or ocular hypertension. Participants are randomized to receive the implant (with sham and placebo controls as appropriate) or topical timolol and are followed for safety and intraocular pressure (IOP) lowering outcomes. Key eligibility includes a diagnosis of open-angle glaucoma or ocular hypertension and excludes eyes with prior incisional glaucoma surgery, prior argon laser trabeculoplasty (ALT), or prior minimally invasive glaucoma surgery (MIGS). The study collects both efficacy endpoints (IOP reduction) and safety data related to the implant and ocular procedures.

Why it matters

Potential benefit: If successful, the implant could provide sustained IOP lowering without daily drops, improving adherence and potentially reducing glaucoma progression risk.

How similar studies have gone: Earlier-generation intracameral prostaglandin implants, including travoprost devices, have demonstrated IOP lowering versus topical therapy in prior trials, though this second-generation implant is a newer iteration undergoing further testing.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Diagnosis of open-angle glaucoma or ocular hypertension 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

Where it's running

  • Glaukos Investigative Site
    Grand Junction, Colorado, United States
    Recruiting
  • Glaukos Investigative Site
    Oklahoma City, Oklahoma, United States
    Recruiting
  • Glaukos Clinical Site
    El Paso, Texas, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.