ABSTRACT:Haemophilia, a group of inherited bleeding disorders, remains a health challenge due to limitations in traditional factor replacement therapy, including frequent infusions and inhibitor development. Asia, particularly China, has emerged as a hub for innovative haemostasis management, with breakthroughs in gene therapy, novel protein activators and targeted biologics. This paper synthesises key advancements: (1) Gene therapy for haemophilia in China; (2) AAV vector engineering and large‐scale manufacturing for haemophilia gene therapy, highlighted by China's first‐in‐Asia clinical trials and global case reports; (3) the FX activator Bemiltenase Alfa (STSP‐0601) for inhibitor‐positive patients and (4) the anti‐APC monoclonal antibody SR604, a precision therapy under phase I/II trials.