Drug Use Investigation for Eylea for Neovascular Glaucoma (NVG)

  • End date
    Jun 30, 2028
  • participants needed
  • sponsor
Updated on 17 October 2022


This is a prospective, observational, multi-center and post-authorization safety study that includes patients with a diagnosis of Neovascular Glaucoma. The investigator will have made the decision to use Eylea for treatment.

The objective of this study is to assess safety and effectiveness of Eylea using in real clinical practice. Patients will be followed for a time period of 6 months from start of Eylea treatment or until it is no longer possible (e.g. lost to follow-up). In total, 480 patients will be recruited. For each patient, data are collected as defined in the electronic case report form (eCRF) at the initial visit, follow-up visit and final visit, either by routine clinical visits (as per investigators routine practice).

Condition Neovascular Glaucoma
Treatment Aflibercept (Eylea, BAY86-5321)
Clinical Study IdentifierNCT04519619
Last Modified on17 October 2022


Yes No Not Sure

Inclusion Criteria

Diagnosis of NVG
Patients who have received IVT-AFL treatment according to Japanese labeling

Exclusion Criteria

Patients who are contraindicated based on approved label
Diagnosis of other indication
Clear my responses

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Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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