Recruiting

Eylea Safety and Effectiveness for Neovascular Glaucoma

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Study Aim

This study aims to observe the safety and effectiveness of Eylea in individuals with neovascular glaucoma by monitoring for adverse events.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Eye Diseases+1

+ Glaucoma

+ Ocular Hypertension

+4 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: November 2020
See protocol details

Summary

Principal SponsorBayer
Study ContactBayer Clinical Trials Contact
Last updated: February 3, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: November 27, 2020

Actual date on which the first participant was enrolled.

This study is focused on understanding how safe and effective the drug Eylea is for treating Neovascular Glaucoma, a serious eye condition that can lead to vision loss. The study involves patients who have already been diagnosed with this condition and whose doctors have chosen Eylea as part of their treatment plan. The main goal is to gather real-world information about how patients respond to Eylea over time, which can help improve future treatment options and care for those affected by this type of glaucoma. Participants in the study will receive Eylea as part of their regular treatment and will be monitored for six months. During this time, researchers will collect detailed information at the start, during regular follow-up visits, and at the end of the study. The primary focus is on recording any adverse events, which are any unexpected problems or side effects that occur during treatment. This information is crucial for determining how safe Eylea is for patients in everyday clinical settings.

Official TitleDrug Use Investigation for Eylea for Neovascular Glaucoma (NVG)
Principal SponsorBayer
Study ContactBayer Clinical Trials Contact
Last updated: February 3, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

480 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Eye DiseasesGlaucomaOcular HypertensionGlaucoma, Neovascular

Criteria

2 inclusion criteria required to participate
Diagnosis of NVG

Patients who have received IVT-AFL treatment according to Japanese labeling.

2 exclusion criteria prevent from participating
Patients who are contraindicated based on approved label

Diagnosis of other indication

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Many locations

Multiple Locations, JapanOpen Many locations in Google Maps
Recruiting
One Study Center
Eylea Safety and Effectiveness for Neovascular Glaucoma | PatLynk