drugset / Trial / NCT02698566
A Study in Patients With Neovascular Age Related Macular Degeneration or Macular Edema Secondary To Retinal Vein Occlusion to Evaluate Usability of the Ranibizumab (Lucentis®) Prefilled Syringe (PFS)
NaSingle-groupOpen-labelOther
Summary
This is a multicenter study designed to evaluate usability of ranibizumab PFS in patients with neovascular age related macular degeneration or macular edema secondary to retinal vein occlusion.
Timeline
- Start
- 2016-03-21
- Primary completion
- 2016-04-05
- Completion
- 2016-04-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Background | Ranibizumab | Monoclonal antibody | 0.5 mg | Intravitreal |