Drug Use Investigation for Eylea for Neovascular Glaucoma (NVG)
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- STATUS
- Recruiting
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- End date
- Jun 30, 2028
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- participants needed
- 480
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- sponsor
- Bayer
Summary
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).
Details
| Condition | Neovascular Glaucoma |
|---|---|
| Treatment | Aflibercept (Eylea, BAY86-5321) |
| Clinical Study Identifier | NCT04519619 |
| Sponsor | Bayer |
| Last Modified on | 17 October 2022 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf 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.
Learn moreComplete 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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