drugset / Trial / NCT03340610
IAI for Persistent DME After Treatment With Bevacizumab And Ranibizumab
NaSingle-groupOpen-labelTreatment
Summary
This is a phase 4 prospective, nonrandomized, open label, interventional clinical trial. Study eyes will receive 5 required initial monthly Intravitreal Aflibercept (IAI) doses of 2 mg followed by 2q8 IAI for a total of 52 weeks; only one study eye from each patient will be enrolled.
Timeline
- Start
- 2015-06
- Primary completion
- 2018-12
- Completion
- 2018-12-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Aflibercept | Protein / enzyme biologic | 2 mg | Intravitreal |