Abstract
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disorder characterized by chronic complement-mediated hemolysis. Eculizumab, a humanized monoclonal antibody against the terminal complement protein C5, potently reduces chronic intravascular hemolysis. We tested the clinical efficacy and safety of a 24-week treatment with eculizumab in 6 Korean patients with PNH.
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CITATION STYLE
Kim, J. S., Lee, J. W., Kim, B. K., Lee, J.-H., & Chung, J. (2010). The use of the complement inhibitor eculizumab (Soliris®) for treating Korean patients with paroxysmal nocturnal hemoglobinuria. The Korean Journal of Hematology, 45(4), 269. https://doi.org/10.5045/kjh.2010.45.4.269
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