作者
Yuri Teranishi-Ikawa,Tetsuhiro Soeda,Hikaru Koga,Kazuki Yamaguchi,K. Katō,Keiko Esaki,Kentaro Asanuma,Miho Funaki,Mina Ichiki,Yuri Ikuta,Shunsuke Ito,Eri Joyashiki,Shunichiro Komatsu,Atsushi Muto,Kei Nishimura,Momoko Okuda,Hisakazu Sanada,Motohiko Sato,Norihito Shibahara,Tetsuya Wakabayashi,Koji Yamaguchi,Akiko Matsusaki,Zenjiro Sampei,Hirotake Shiraiwa,Hiroko Konishi,Yoshiki Kawabe,Kunihiro Hattori,Takehisa Kitazawa,Tomoyuki Igawa
摘要
Emicizumab, a factor (F) VIIIa-function mimetic bispecific antibody (BsAb) to FIXa and FX, has become an indispensable treatment option for people with hemophilia A (PwHA). However, a small proportion of PwHA still experience bleeds even under emicizumab prophylaxis, as observed in the long-term outcomes of clinical studies. A more potent BsAb may be desirable for such patients.