A Study Of The Effectiveness And Safety Of A 36-Week Refill Regimen For The Port Delivery System With Ranibizumab Vs Aflibercept Treat & Extend In Subjects With Neovascular Age-Related Macular Degeneration
Stopped Roche/Genentech has initiated an immediate pause of all new PDS implantations because the implants from commercial supply in the clinical studies did not meet the filed specifications for the intended use
Conditions
- Neovascular Age-Related Macular Degeneration
Interventions
- DRUG: Ranibizumab
- DRUG: Aflibercept
- DEVICE: Port Delivery System with ranibizumab (PDS)
Sponsor
Hoffmann-La Roche