Long-term efficacy and safety of eculizumab in Japanese patients with PNH: AEGIS trial Yuzuru KanakuraKazuma OhyashikiTsutomu ShichishimaShinichiro Okamoto • Kiyoshi AndoHaruhiko NinomiyaTatsuya KawaguchiShinji NakaoHideki Nakakuma • Jun-ichi NishimuraTaroh KinoshitaCamille L. BedrosianKeiya OzawaMitsuhiro Omine

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, progressive hematopoietic stem cell disorder char- acterized by chronic complement-mediated hemolysis leading to life-threatening complications and early mor- tality. Eculizumab, a humanized anti-C5 monoclonal anti- body, inhibits terminal complement activation, reduces hemolysis, decreases the risk of thrombosis, and improves renal function and quality of life in PNH patients. The long-term efficacy and safety of eculizumab in Japanese patients were assessed in a 2-year extension to a 12-week, open-label study (AEGIS). Eculizumab treatment led to an immediate and sustained reduction in intravascular hemolysis (P \ 0.001) and red blood cell transfusions (P = 0.0016) compared with baseline levels. There were no reports of thromboembolism during eculizumab treat- ment. The majority of patients had stable (56 %) or improved (41 %) renal function and an improved quality of life (P = 0.015), with sustained reductions in fatigue and dyspnea. Eculizumab was well tolerated; no deaths or serious hemolytic events were reported, and the rate of infections declined over time. There were no significant differences in the response to eculizumab in patients with or without bone marrow dysfunction. These results dem- onstrate that eculizumab is an effective, well-tolerated