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A Long-term Follow-Up Study to Evaluate the Safety and Efficacy of Suprachoroidal Administration of RGX-314 for Participants With Neovascular Age-Related Macular Degeneration

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Trial Profile

A Long-term Follow-Up Study to Evaluate the Safety and Efficacy of Suprachoroidal Administration of RGX-314 for Participants With Neovascular Age-Related Macular Degeneration

Status: Recruiting
Phase of Trial: Phase II

Latest Information Update: 13 Aug 2026

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At a glance

  • Drugs Surabgene lomparvovec (Primary)
  • Indications Wet age-related macular degeneration
  • Focus Adverse reactions
  • Sponsors REGENXBIO

Most Recent Events

  • 05 Aug 2026 Planned number of patients changed from 115 to 116.
  • 05 Aug 2026 Planned End Date changed from 1 Mar 2028 to 1 Jul 2031.
  • 05 Aug 2026 Planned primary completion date changed from 1 Mar 2028 to 1 Jul 2031.

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