drugset / Trial / NCT04993352
Evaluate the Safety and Efficacy of HLX04-O in Subjects With wAMD
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bevacizumab | Monoclonal antibody | 1.25 mg | Intravitreal |