drugset / Trial / NCT04522167
Efficacy and Safety of the Aflibercept FYB203 Biosimilar in Comparison to Eylea® in Patients With Neovascular Age-Related Macular Degeneration
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This is a randomized, double-masked, multicenter study to evaluate the efficacy and safety of FYB203 compared to Eylea® in patients with neovascular age related macular degeneration.
Timeline
- Start
- 2020-07-21
- Primary completion
- 2022-06-23
- Completion
- 2023-05-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Aflibercept | Protein / enzyme biologic | 2 mg | Intravitreal |
| Comparator | Aflibercept | Protein / enzyme biologic | 2 mg | — |