drugset / Trial / NCT02441816
VITAL - Individualising Therapy for Neovascular AMD With Aflibercept
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to assess a new treatment pattern for aflibercept. The aim is to achieve and maintain the best benefit of visual function and avoid unnecessary hospital visits. The hypothesis to be tested is whether intravitreous aflibercept given in an 8 week cycle of treatment in year 1 and a capped treat and extend treatment paradigm in year 2 can lead to improved vision and reading speed in eyes with active wet AMD over 2 years while reducing hospital visits.
Timeline
- Start
- 2014-11
- Primary completion
- 2018-01-26
- Completion
- 2018-01-26
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Aflibercept | Protein / enzyme biologic | 2 mg | Intravitreal |