Your session is about to expire
← Back to Search
Travoprost for Open-Angle Glaucoma
Phase 2
Waitlist Available
Research Sponsored by Glaukos Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months
Awards & highlights
Study Summary
This study is evaluating whether the surgical procedure is safe for people with glaucoma or ocular hypertension.
Eligible Conditions
- Open-Angle Glaucoma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Ocular Safety
Secondary outcome measures
Anterior Chamber Cells
Anterior Chamber Flare
Corneal Edema
+14 moreSide effects data
From 2019 Phase 3 trial • 565 Patients • NCT0291450938%
Adverse Event
1%
Serious Adverse Event
100%
80%
60%
40%
20%
0%
Study treatment Arm
Placebo Vehicle (PV)
OTX-TP (Sustained Release Travoprost) Intracanalicular Depot
Trial Design
1Treatment groups
Experimental Treatment
Group I: Implantation and ExchangeExperimental Treatment1 Intervention
Subjects will undergo implantation and exchange of a Travoprost Intraocular Implant through a small temporal clear corneal incision.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Travoprost
FDA approved
Find a Location
Who is running the clinical trial?
Glaukos CorporationLead Sponsor
65 Previous Clinical Trials
9,007 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Share this study with friends
Copy Link
Messenger