A Multicenter, Open-Label Extension Study to Evaluate the Long-Term Safety and Tolerability of the Port Delivery System With Ranibizumab in Patients With Neovascular Age-Related Macular Degeneration (Portal)
Latest Information Update: 01 Apr 2026
At a glance
- Drugs Ranibizumab (Primary) ; Ranibizumab (Primary)
- Indications Wet age-related macular degeneration
- Focus Adverse reactions
- Acronyms Portal
- Sponsors Roche
Most Recent Events
- 05 Jan 2026 Planned End Date changed from 30 Sep 2029 to 31 Oct 2029.
- 05 Jan 2026 Planned primary completion date changed from 30 Sep 2029 to 31 Oct 2029.
- 04 Sep 2025 According to a Roche media release, Susvimo (ranibizumab injection, 100 mg/mL) is currently under review by the European Medicines Agency (EMA) for the treatment of neovascular age-related macular degeneration (nAMD). The EMA's evaluation is based on data from the pivotal Phase III Archway trial, the Phase II LADDER study, and an open-label long-term extension study.