Introduction: The factor VIII (FVIII)-mimetic bispecific monoclonal antibody, emicizumab, previously approved for prophylaxis in haemophilia A with inhibitors, has been recently licensed in several countries also in patients with severe haemophilia A (PWSHA) without inhibitors. The introduction of this innovative agent requires the development of specific pathways at Haemophilia Treatment Centres (HTC), particularly regarding laboratory testing and treatment of breakthrough bleeds and invasive procedures/surgeries, even more critical when patients are managed by non-specialist professionals. Limited literature data and clinical experience in PWSHA without inhibitors on emicizumab are currently available. Aim: To promote awareness and overco...
Emicizumab is a bispecific antibody that activates FX to FXa in the absence of FVIII. It has been sh...
Emicizumab (Hemlibra®) recently became available and requires an adaptation for managing bleeding, s...
International audienceIntroduction Emicizumab (Hemlibra (R)) recently became available and requires ...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab is a recombinant, humanized, bispecific, asymmetric monoclonal antibody that bridges acti...
Emicizumab is a recombinant, humanized, bispecific, asymmetric monoclonal antibody that bridges acti...
Emicizumab is a bispecific antibody that activates FX to FXa in the absence of FVIII. It has been sh...
Emicizumab (Hemlibra®) recently became available and requires an adaptation for managing bleeding, s...
International audienceIntroduction Emicizumab (Hemlibra (R)) recently became available and requires ...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab has been approved in several countries for regular prophylaxis in patients with congenita...
Emicizumab is a recombinant, humanized, bispecific, asymmetric monoclonal antibody that bridges acti...
Emicizumab is a recombinant, humanized, bispecific, asymmetric monoclonal antibody that bridges acti...
Emicizumab is a bispecific antibody that activates FX to FXa in the absence of FVIII. It has been sh...
Emicizumab (Hemlibra®) recently became available and requires an adaptation for managing bleeding, s...
International audienceIntroduction Emicizumab (Hemlibra (R)) recently became available and requires ...