Eculizumab is a monoclonal antibody that targets complement protein C5. Binding to this protein prevents the activation of a complement terminal complex, which is used to treat a number of autoimmune conditions.
Eculizumab was granted FDA approval on 16 March 2007. In Q1 2023, the EMA's Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion of two formulations of eculizumab indicated for the treatment of paroxysmal nocturnal hemoglobinuria.
Eculizumab is indicated in the US to treat paroxysmal nocturnal hemoglobinuria (PNH) to reduce hemolysis, atypical hemolytic uremic syndrome to inhibit complement-mediated thrombotic microangiopathy, and neuromyelitis optica spectrum disorder (NMOSD). It is also indicated in EU to treat PNH in both adult and pediatric patients.
Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, Beijing, China
Chinese Academy of Medical Sciences Hematology Hospital, Tianjin, Tianjin, China
Huashan Hospital, Shanghai, Shanghai, China
The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China
Research Site, Wuhan, China
Research Site, Wuhan, China
Research Site, Zhengzhou, China
Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, Beijing, China
The Blood Disease Hospital of the Chinese Academy of Medical Sciences, Tianjin, Tianjin, China
Peking University First Hospital, Beijing, China
West China Hospital, Sichuan University, Chengdu, Sichuan, China
Research Site, Wuhan, China
Research Site, Wuhan, China
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