Trials / Recruiting
RecruitingNCT04519619
Study to Learn More About Safety of Aflibercept Injection in Japanese Patients With Neovascular Glaucoma (NVG)
Drug Use Investigation for Eylea for Neovascular Glaucoma (NVG)
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 480 (estimated)
- Sponsor
- Bayer · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
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).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Aflibercept (Eylea, BAY86-5321) | Administration by intravitreal injection |
Timeline
- Start date
- 2020-11-27
- Primary completion
- 2027-06-30
- Completion
- 2028-06-30
- First posted
- 2020-08-19
- Last updated
- 2026-03-31
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT04519619. Inclusion in this directory is not an endorsement.