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Study to Assess the Injection Burden, Adverse Events, Change in Disease Activity, and Long-Term Preservation of Visual Acuity of Surabgene Lomparvovec in Adult Participants With Neovascular Age-Related Macular Degeneration (nAMD)

Study on injections, side effects, and vision impact in nAMD patients.

Recruiting
50 years and older
All
Phase 3
The study investigates **Surabgene Lomparvovec**, a potential treatment for **neovascular age-related macular degeneration (nAMD)**, also known as "wet" AMD. This condition involves the growth of abnormal blood vessels in the retina, which is the light-sensitive part at the back of the eye. In this study, adults aged 50 and older who have been previously treated for nAMD will participate. Participants will be divided into three groups. Groups 1 and 2 will receive a single dose of the gene therapy Surabgene Lomparvovec as an injection between the retina and the back of the eye. Group 3 will receive a different treatment called **Ranibizumab**, injected into the jelly-like part inside the eye. The study will assess the treatment over a period of up to 5 years, requiring regular monthly visits to a hospital or clinic for medical assessments, blood tests, and questionnaires.
  • Participation involves regular monthly visits over up to 5 years.
  • Participants may receive different treatments based on group assignment.
  • Medical assessments and questionnaires are part of the study.
Study details
    Neovascular Age-related Macular Degeneration

NCT07007065

AbbVie

19 September 2026

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