复宏汉霖高级副总裁兼首席商务发展官曹平女士在BIO主题演讲中强调：公司成立以来始终践行为患者提供高质量且可负担的创新药物的使命，全球累计惠及患者超80万例，实现从研发到商业化的价值闭环。复宏汉霖首席技术官、高级副总裁许圣昌博士聚焦复宏汉霖在AI辅助药物开发领域的突破性进展进行了介绍，印证了公司"创新-可及"双引擎发展路径的国际竞争力。此外，在公司协办的“BlOCHINA Global Forum 2025@Boston”中国生物药国际化论坛上，曹平女士与公司总裁黄玮女士携手全球合作伙伴Accord、Dr.Reddy's、Palleon、Organon、Sermonix，分享与中国生物制药企业合作的核心驱动力和战略考量，全面展示了公司的国际化合作布局，引发业界的高度聚焦与广泛赞誉，进一步增强了公司在全球生物医药市场的影响。

复宏汉霖以患者需求为根基，以创新为引擎，以全球化为驱动，依托前沿的生产与质量体系和卓越的商业化运营能力，致力于为全球患者提供可负担的高品质生物药。公司就汉曲优^®（美国商品名：HERCESSI^™，欧洲商品名：Zercepac^®）、H药 汉斯状^®（斯鲁利单抗，欧洲商品名：Hetronifly^®）、汉利康^®、HLX11、HLX14、HLX15等多个产品，携手Accord、Abbott、Dr.Reddy’s、Eurofarma、KGbio、Sandoz和Organon等国际一流的生物制药企业拓展全球市场，授权区域全面覆盖欧美主流生物药市场和众多新兴市场。

汉曲优^®是在中美欧三地皆获批的“中国籍”单抗生物类似药，现已在超过50个国家和地区获批上市，其商业化供货网络已覆盖中国、东南亚、北美、欧洲、中东及拉丁美洲等地区，惠及超过25万名患者。公司另一款抗肿瘤核心产品H药 汉斯状^®是全球首个获批用于一线治疗小细胞肺癌（SCLC）的抗PD-1单抗，已在中国、欧洲及东南亚等30余个国家和地区获批上市。同时，H药治疗SCLC也已获得美国FDA、欧盟EC、瑞士Swissmedic的孤儿药资格认定，并获韩国MFDS授予ES-SCLC孤儿药资格，有望惠及全球更广泛的肿瘤患者群体。与此同时，公司高效推进创新管线产品的临床进展，创新型抗HER2单抗HLX22的国际多中心III期研究同步于中国、澳大利亚、欧盟、日本、美国、南美洲等国家和地区开展。潜在同类首创/最优产品HLX43（PD-L1 ADC）的国际多中心II期临床研究于中国完成首例受试者给药，是全球首个进入临床II期的靶向PD-L1的ADC产品。

未来，复宏汉霖将继续携手全球合作伙伴，通过创新与合作，为全球患者带来更多优质、可负担的治疗选择。

Henlius Shines at 2025 BIO International Convention, Showcasing Its Innovative Achievements

From June 16-19, 2025, the 2025 BIO International Convention (“BIO 2025”) was held at the Boston Convention & Exhibition Center in Boston, Massachusetts, USA. Marking its seventh consecutive year at the conference, Henlius showcased a wide range of innovative research and development accomplishments, attracting significant attention from numerous attendees and organizations. During the conference, Henlius held around 130 in-depth meetings, driving exchanges on collaboration opportunities for in-licensing, research collaboration, or commercial right out-licensing. 

Ping Cao, Henlius SVP and Chief Business Development Officer, emphasized in her BIO keynote: Henlius has delivered on its mission to provide high-quality and affordable biologics since inception, benefiting over 800,000 patients globally while achieving end-to-end value integration from R&D to commercialization. Simon Hsu, CTO and SVP of Henlius, highlighted breakthroughs in AI-driven drug development, demonstrating how Henlius' double engines of innovation and accessibility fuel its global competitiveness. Additionally, at the 'BIO CHINA Global Forum 2025@Boston' co-hosted by Henlius, the company's executives engaged in in-depth discussions with global partners Accord, Dr. Reddy's, Palleon, Organon, and Sermonix on strategic drivers for global partnerships with Chinese biopharma, showcasing our international footprint. The dialogue sparked significant industry attention and further amplified the company's global influence in the biologics market.

Henlius anchors its strategy in unmet patient needs, powers progress through continuous innovation and advances its global presence with manufacturing and quality systems, as well as commercialization capabilities, delievering the goals of providing innovative and affordable biologics for global patients. The company has expanded its global market presence with several products, including HANQUYOU, HANSIZHUANG, HANLIKANG, HLX11, HLX14, and HLX15, in collaboration with renowned international biopharmaceutical companies such as Accord, Abbott, Dr.Reddy’s, Eurofarma, KGbio, Sandoz and Organon. It has achieved comprehensive coverage in the mainstream biopharmaceutical markets of Europe, the United States, and numerous emerging markets, contributing to the global development of China's biopharmaceutical innovation.

Henlius’ self-developed and manufactured trastuzumab biosimilar HANQUYOU (trade name: HERCESSI™ in U.S. and Zercepac^® in Europe) is a China-developed mAb biosimilar approved in China, Europe, and U.S. It has been approved in over 50 countries and regions, covering China, Southeast Asia, North America, the EU, Middle East, and Latin America, benefiting over 250,000 patients. Additionally, the company prides itself on its HANSIZHUANG (serplulimab, trade name: Hetronifly ® in Europe), the world's first anti-PD-1 mAb for the first-line treatment of small cell lung cancer (SCLC), and it has been approved in more than 30 countries and regions, including China, the EU, and Southeast Asia. To date, Orphan Drug Designation (ODD) granted to HANSIZHUANG for the treatment of SCLC by U.S. FDA, EC, and Swissmedic, and for Extensive-Stage SCLC (ES-SCLC) by Korea MFDS. Meanwhile, the company is efficiently advancing the clinical progress of its innovative product portfolio. The phase 3 international multicentre clinical trails of Henlius' novel anti-HER2 mAb, HLX22, is being conducted simultaneously across China, Australia, the European Union, Japan, the United States, South America, and other countries and regions. Recently, the first subject has been dosed for a phase 2 international muticenter clinical trial of HLX43（PD-L1 ADC）, another company’s potential first/best-in-class products. At present, HLX43 is the first PD-L1 ADC progressed to phase 2 clinical trial development globally.

Looking forward, Henlius will continue to collaborate closely with global partners, leveraging innovation and cooperation, to deliver more high-quality, affordable treatment options to patients worldwide.

媒体：PR@Henlius.com

投资者：IR@Henlius.com