drugset / Trial / NCT03777332

Study to Evaluate the Safety of Intravitreal APL-2 in Patients Diagnosed With Geographic Atrophy

NCT03777332

Phase 1 Completed 19 enrolled Apellis Pharmaceuticals, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Safety Assessment of APL-2 in Patients with Geographic Atrophy

Timeline

Start
2018-11-05
Primary completion
2021-04-01
Completion
2021-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Pegcetacoplan Peptide 15 mg Intravitreal