A Long-term Follow-Up Study to Evaluate the Safety and Efficacy of RGX-314 Following Subretinal Administration in Participants With Neovascular Age-related Macular Degeneration and Fellow Eye Treatment Substudy
Latest Information Update: 24 May 2023
At a glance
- Drugs Surabgene lomparvovec (Primary)
- Indications Wet age-related macular degeneration
- Focus Adverse reactions
- Acronyms RGX-314 LTFU
- Sponsors AbbVie; REGENXBIO
Most Recent Events
- 29 Mar 2023 According to ClinicalTrials.gov record, protocol has been amended to increase patient number from 42 to 865, treatment arm changed from 1 to 2. Official title is changed and so the age criteria from 18 years to 50 years. Study design is now Single Group Assignment and addition of new primary endpoint.
- 29 Mar 2023 Planned number of patients changed from 42 to 865.
- 29 Mar 2023 Planned End Date changed from 1 Jun 2024 to 1 Dec 2028.