Trial to Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant
← catalyst calendarNCT07495852 · readout ≤ 681 d
Sponsored by Glaukos Corporation (industry) · GKOS — their whole pipeline →.
Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
510estimated
Sites
1
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-02-17 | actual | When the study began enrolling |
| Primary completion | Jun 2028 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | Mar 2032 | estimated | The whole study's end, after follow-up |
| First posted | 2026-03-27 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-03-30 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Glaucoma
Interventions
- Drug: Gen 2 Travoprost Intracameral Implant — also filed as Gen 2 Travoprost Intraocular Implant
- Drug: Timolol eye drops 0.5% — also filed as Timolol maleate ophthalmic solution, 0.5%
- Procedure: Sham Procedure
- Other: placebo eye drops
Primary outcome
what the primary-completion date above is the date OFIntraocular pressure (IOP)
measured 3 months
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