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Beta Blocker
Travoprost Intraocular Implant, high elution 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
Open angle glaucoma
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up post-op through month 36
Awards & highlights
Study Summary
This study is evaluating whether a higher dose of the Travoprost Intraocular implant is more effective than a lower dose.
Eligible Conditions
- Open-Angle Glaucoma
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ post-op through month 36
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post-op through month 36
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
IOP (mmHg) Change From Baseline at Week 12
Other outcome measures
Severe Adverse Events
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: Travoprost Intraocular Implant, low elutionExperimental Treatment1 Intervention
This implant will be surgically implanted and elute travoprost, a prostaglandin.
Group II: Travoprost Intraocular Implant, high elutionExperimental Treatment1 Intervention
This implant will be surgically implanted and elute travoprost, a prostaglandin.
Group III: Timolol Maleate Ophthalmic Solution, 0.5%Active Control1 Intervention
Timolol, a beta blocker, will be dosed twice daily
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Travoprost
FDA approved
Travoprost
FDA approved
Find a Location
Who is running the clinical trial?
Glaukos CorporationLead Sponsor
65 Previous Clinical Trials
8,886 Total Patients Enrolled
Kerry Stephens, O.D.Study ChairGlaukos Corporation
4 Previous Clinical Trials
1,665 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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