Gen 2 Travoprost Intracameral Implant
Drugtravoprost
Other names: Gen 2 Travoprost Intraocular Implant
NCT Number: NCT07075718
Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Glaukos Investigative Site, Grand Junction, Colorado, United States
Evaluate the Safety and Efficacy of the Second Generation Travoprost Intracameral Implant Compared to Timolol Ophthalmic Solution 0.5% Administered Twice Daily in Subjects with Open-Angle Glaucoma or Ocular Hypertension
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
travoprost
Other names: Gen 2 Travoprost Intraocular Implant
timolol 0.5%
Other names: Timolol maleate ophthalmic solution, 0.5%
sham implant administration
artificial tears
Time frame: 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
Contact information is provided by the study sponsor or research team.
Glaukos Corporation
Industry
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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