Overview

Evaluate the Safety and Efficacy of HLX04-O in Subjects With wAMD

Status:
Recruiting
Trial end date:
2023-04-01
Target enrollment:
Participant gender:
Summary
This study will evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of HLX04-O administered every 4 weeks in participants with wet age-related macular degeneration (wAMD)
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Shanghai Henlius Biotech
Treatments:
Antibodies
Antibodies, Monoclonal
Endothelial Growth Factors
Mitogens