Clinical Trial

Lesion-tailored, Fundus-controlled Perimetry in Geographic Atrophy (GA).

Study acronym: FCPGA-2025
Recruiting
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Summary
The goal of this observational study is to evaluate changes in retinal sensitivity over time in patients with geographic atrophy due to age related macular degeneration who are receiving pegcetacoplan as part of routine clinical care. The study aims to determine whether lesion tailored fundus-controlled perimetry can reliably measure functional changes near areas of atrophy and whether this testing can be implemented in everyday clinic care over 24 months. Participants will undergo repeated vision testing, standard eye imaging, and visual function questionnaires while continuing their prescribed treatment.
Protocol Amendment History 2 changes
critical Recruitment opened 2026-06-18
critical Primary endpoint(s) modified 2026-05-15
Trial Details
NCT Number NCT07582042
Lead Sponsor University of Utah
Collaborators: Apellis Pharmaceuticals, Inc.
Conditions Geographic Atrophy From Age-related Macular Degeneration
Enrollment 50 participants
Start Date 2026-06-15
Primary Completion 2029-05-01 (estimated)
Study Completion 2029-08-01 (estimated)
Updated on ClinicalTrials.gov 2026-06-17