Overview

Assessment of Safety, Tolerability and Pharmacokinetics of Intravitreal Pegcetacoplan (APL-2) for Patients With Wet AMD

Status:
Completed
Trial end date:
2016-03-08
Target enrollment:
Participant gender:
Summary
The objective of this study is to provide initial safety, tolerability and pharmacokinetics information of intravitreal administration of pegcetacoplan in order to support further development into larger Phase II studies for treatment of patients with AMD.
Phase:
Phase 1
Details
Lead Sponsor:
Apellis Pharmaceuticals, Inc.