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Clinical Trial Summary

Subjects with secondary wet age-related macular degeneration(AMD) or recurrent subfoveal choroidal neovascularization (CNV) in only one study eye will be enrolled into the study.


Clinical Trial Description

The screening period was 28 days. The classification of CNV will be determined by Fundus Fluorescein Angiography ( FFA ) at the study centers. Subjects will receive intravitreal injections of TAB014 Monoclonal Antibody Injection in one eye ( the study eye ). Subjects will only receive single intravitreal dose. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03675880
Study type Interventional
Source Lee's Pharmaceutical Limited
Contact youxin chen, PHD
Phone 010-69156699
Email chenyouxinpumch@163.com
Status Recruiting
Phase Phase 1
Start date June 15, 2018
Completion date April 30, 2019

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