drugset / Trial / NCT04993352

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

NCT04993352 ↗

Phase 1/2 Completed 20 enrolled Shanghai Henlius Biotech
NaSingle-groupOpen-labelTreatment

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)

Timeline

Start
2021-07-15
Primary completion
2022-07-07
Completion
2023-03-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 1.25 mg Intravitreal