Geographic Atrophy Clinical Trial
Official title:
A Phase II, Multicenter, Randomized, Single-Masked, Sham-Controlled Study of Safety, Tolerability and Evidence of Activity of Intravitreal APL-2 Therapy in Patients With Geographic Atrophy (GA)
The primary objectives of the study are to assess the safety, tolerability and evidence of activity of multiple intravitreal (IVT) injections of pegcetacoplan in subjects with Geographic Atrophy associated with Age-Related Macular Degeneration (AMD).
This is a Phase II, prospective, multicenter, randomized, single-masked, sham-controlled
study to assess the safety, tolerability and evidence of activity of multiple IVT injections
of pegcetacoplan in subjects with GA secondary to Age-Related Macular Degeneration.
The study will randomize approximately 240 subjects to obtain at least 200 evaluable subjects
across 40 multinational sites.
Subjects will be randomized in a 2:2:1:1 manner to receive pegcetacoplan Monthly (AM),
pegcetacoplan Every-Other-Month (AEOM), Sham injection Monthly (SM) or Sham injection
Every-Other-Month (SEOM), respectively.
All subjects will return to the clinical site on Day 7 to assess acute safety after the first
injection. After that, subjects in the monthly groups will return to the clinical site for
additional pegcetacoplan (or Sham) injections and study procedures every month until Month
12. Subjects in the Every-Other-Month groups will return to the clinical site for additional
pegcetacoplan (or Sham) injections and study procedures every two months until Month 12. All
subjects will return for follow-up visits on Months 15 and 18 (3 and 6 months after last
injection, respectively).
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