A Phase III Multi-Center Randomized Double-Masked Active- and Placebo-Controlled Study of Trabodenoson in Adults with Ocular Hypertension or Primary Open-Angle Glaucoma
Study on Investigational Medication for Ocular Hypertension or Primary Open-Angle Glaucoma
Brief description of study.
The purpose of this study is to gather information about an investigational drug called trabodenoson which was found to increase the outflow capabilities of the eye in a Phase 2 study in patients with OHT or POAG.
Detailed description of study
The purpose of this study is to gather information about an investigational drug called trabodenoson which was found to increase the outflow capabilities of the eye in a Phase 2 study in patients with Ocular Hypertension or Primary Open-Angle Glaucoma.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Ocular Hypertension
-
Age: 18 years - 100 years
-
Gender: All
This study investigates an investigational medication that may help increase the fluid outflow in the eyes of patients. The study focuses on individuals with Ocular Hypertension (OHT) or Primary Open-Angle Glaucoma (POAG), which are conditions that can affect eye pressure and vision.
Participants in this study will undergo procedures to assess the effectiveness of the investigational medication in managing their eye conditions. These procedures are designed to measure changes in eye pressure and fluid outflow.
- Who can participate: Individuals diagnosed with Ocular Hypertension or Primary Open-Angle Glaucoma may be eligible to participate. Specific age criteria and other factors are not specified, or it is open to all ages if applicable.
- Study details: Participants will receive either the investigational medication or a placebo, which is an inactive substance that looks like the investigational medicine but does not contain any medicine. The study will involve regular monitoring of eye health.
Interested in the study?
Select a study center that’s convenient for you, and get in touch with the study team.
Please choose between Voice or SMS based delivery of verification code
or