drugset / Trial / NCT03335852

Safety and Pharmacokinetics of Abicipar Pegol Intravitreal Injections in Japanese Patients With Neovascular AMD

NCT03335852

Phase 1 Completed 11 enrolled Allergan
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety and to characterize the systemic pharmacokinetics of free and vascular endothelial growth factor (VEGF)-bound abicipar following multiple monthly intravitreal injections of abicipar in Japanese patients with neovascular age-related macular degeneration (AMD).

Timeline

Start
2017-11-28
Primary completion
2018-10-08
Completion
2018-10-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Abicipar pegol Protein / enzyme biologic 2 mg Intravitreal

Indications