drugset / Trial / NCT03525613

A Study to Compare the Efficacy and Safety of Intravitreal APL-2 Therapy With Sham Injections in Patients With Geographic Atrophy (GA) Secondary to Age-Related Macular Degeneration

NCT03525613 ↗

Phase 3 Completed 637 enrolled Apellis Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a 24-month, Phase III, multicenter, randomized, double-masked, sham-injection controlled study to assess the efficacy and safety of multiple IVT injections of APL-2 in subjects with GA secondary to AMD.

Timeline

Start
2018-08-31
Primary completion
2021-06-28
Completion
2022-06-28

Outcome

Met primary endpoint

registry analysis (superiority test); Pegcetacoplan Monthly vs Sham Pooled; p = 0.0004; LS Mean Difference -0.4114 (95% CI -0.6397 to -0.1831); MMRM model NCT03525613 ↗

registry analysis (superiority test); Pegcetacoplan EOM vs Sham Pooled; p = 0.0055; LS Mean Difference -0.3180 (95% CI -0.5423 to -0.0937); MMRM model NCT03525613 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Pegcetacoplan Peptide 15 mg Intravitreal