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远大医药人工血管海外关键性临床获得新进展

Group 1 - The company, YuanDa Pharmaceutical, has reported positive data from its overseas pivotal clinical trial (aXessEU) for the aXess artificial blood vessel, indicating its market potential in the field of hemodialysis treatment [2][4] - aXess is an innovative endogenous tissue repair product designed for establishing arteriovenous grafts (AVG) for patients with end-stage renal disease (ESRD), utilizing endogenous tissue repair (ETR) technology to facilitate natural vascular recovery [2][3] - The aXessEU study is a prospective trial conducted across 18 centers in Europe, aimed at evaluating the patency, safety, and performance of aXess in ESRD patients requiring vascular access for hemodialysis, showing improvements over standard therapies in all key clinical metrics [2][3] Group 2 - The global hemodialysis market reached approximately $94.43 billion in 2022 and is projected to grow at a compound annual growth rate (CAGR) of about 6.8%, reaching $158.04 billion by 2030 [3] - In China, the number of patients receiving hemodialysis treatment was around 844,300 in 2022, with an estimated market size for the upstream hemodialysis industry (including equipment and consumables) expected to reach nearly 48.4 billion yuan by 2030 [3] - Despite significant market demand, the hemodialysis field has seen slow technological innovation, leaving patients facing unmet clinical needs such as access failure and infections, which aXess aims to address [3]