
汉曲优®启航美国,将为北美患者带来高质量、可负担的治疗选择。

复宏汉霖产品首次发货美国,实现中国、东南亚、北美、欧洲、中东及拉丁美洲等地区商业化供货。

汉曲优®已在50个国家和地区获批上市,惠及逾22万名患者。
11月29日,复宏汉霖自主研发和生产的曲妥珠单抗生物类似药汉曲优®(美国商品名:HERCESSI™,欧洲商品名:Zercepac®)正式从公司松江基地(一)发出,启程运往美国市场。这标志着复宏汉霖首次商业化供货至北美地区,是其全球化战略布局的又一重要突破。至此,复宏汉霖商业化供货网络已成功拓展至中国、东南亚、北美、欧洲、中东及拉丁美洲等地区。
复宏汉霖总裁黄玮女士
美国是全球最大的生物药市场,对药品的供应体系以及企业的综合实力有着严格的要求。此次汉曲优®成功进入美国市场,不仅进一步拓展了复宏汉霖的国际版图,也为公司其他产品的全球化奠定了坚实基础。自汉曲优®2020年开启商业发货至今,我们已完成全球商业化发货约650万支,持续提升生产供应能力,为惠及更多患者不懈努力。
复宏汉霖首席质量官兼副总裁叶峰博士
高质量是企业在国际舞台上站稳脚跟的关键,是赢得客户信任的底气,是产品迈向全球市场的必备条件。药品质量直接关系到每位患者的生命,高质量更是我们造福全球更多患者的坚实基础。我们始终坚持以国际最高标准践行汉霖质量,致力于为更多患者提供高品质的生物药。

汉曲优®是在中国、欧盟、美国获批的“中国籍”单抗生物类似药,现已成功于美国、英国、加拿大、法国、德国、瑞士、澳大利亚、芬兰、西班牙、阿根廷、沙特阿拉伯、泰国等50个国家和地区获批上市,并进入中国、英国、法国和德国等多个国家的医保目录。截至目前,汉曲优®已惠及全球超过22万名HER2阳性乳腺癌和胃癌患者。汉曲优®深入的国际化布局,得益于复宏汉霖长期以来对产品质量的不懈追求。当前,复宏汉霖已建立一套符合国际质量标准的质量管理体系,徐汇基地、松江基地(一)及松江基地(二)三大生产基地及其质量管理体系已通过约100项各国药监机构及国际商业合作伙伴实施的核查及审计,获得中国、美国、欧盟、PIC/S成员印尼及巴西等国家和地区的GMP认证,为产品的全球化供应打下了坚实基础。
此次汉曲优®成功发货美国是基于公司与国际合作伙伴Intas及其子公司Accord达成的独家商业化合作。围绕汉曲优®,复宏汉霖携手商业合作伙伴Accord、Abbott、Eurofarma和KGbio等国际一流的生物制药企业,前瞻性地开展了全球商业化布局。未来,复宏汉霖将继续深化与全球合作伙伴的协作,推进更多高品质药物的全球上市进程,惠及更多患者。
关于复宏汉霖
First Shipment of
Henlius Trastuzumab to U.S.
HANQUYOU shipped to the United States, offering high-quality, affordable treatment options to North American patients -
Henlius' first product exported to the U.S., enabling commercial supply to regions including China, Europe, Latin America, the Middle East, North America, and Southeast Asia -
HANQUYOU approved in 50 countries and regions, benefiting over 220,000 patients -
On November 29, 2024, Henlius' independently developed and produced trastuzumab biosimilar, HANQUYOU (trade name: HERCESSI™ in the U.S. and Zercepac® in Europe), departed from Henlius’ Songjiang First Plant, heading to the U.S. This milestone marks the company’s first commercial supply to North America, representing a significant breakthrough in its global expansion. With this achievement, Henlius has successfully extended its commercial supply network to include China, Europe, Latin America, the Middle East, North America and Southeast Asia.
Ms. Wei Huang, President of Henlius, stated that, “The U.S., as the world's largest biopharmaceutical market, imposes stringent requirements on drug supply systems and the comprehensive strengths of companies. The successful entry of HANQUYOU into the U.S. market not only expands our international footprint but also lays a solid foundation for the globalization of our other products. Since the commercial launch of HANQUYOU in 2020, we have successfully shipped approximately 6.5 million units globally, continuously enhancing our production and supply capabilities in our relentless effort to benefit more patients.”
Dr. Frank Ye,Vice President and Chief Quality Officer, stated that, “High quality is the key to establishing a firm foothold on the global stage, earning customer trust, and enabling products to succeed in international markets. More importantly, it serves as the solid foundation for us to benefit more patients worldwide as medicine quality directly impacts patient lives. At Henlius, we remain committed to upholding the highest international standards of quality, delivering high-quality biologics to even more patients.”
HANQUYOU is a China-developed mAb biosimilar approved in China, the European Union (EU) and U.S. It is now approved in 50 countries and regions including the U.S., United Kingdom (UK), Canada, France, Germany, Switzerland, Australia, Finland, Spain, Argentina, Saudi Arabia, and Thailand, and it is reimbursed nationally in countries and regions including China, the UK, France and Germany. To date, HANQUYOU has benefited over 220,000 patients with HER2 positive breast and gastric cancer worldwide.
HANQUYOU’s extensive global reach is a testament to Henlius' relentless pursuit of excellence in product quality. Henlius has established a quality management system that meets international standards. Its three production sites – Xuhui Facility, Songjiang First Plant and Songjiang Second Plant – along with their quality management systems, have successfully passed approximately 100 inspections and audits conducted by regulatory agencies and international business partners across various countries. The company has been GMP-certified by China, the U.S., the EU as well as PIC/S member countries such as Indonesia and Brazil, equipped with a solid foundation for the global supply of its products.
The successful U.S. launch of HANQUYOU also dates from Henlius' exclusive partnership with Intas and its subsidiary, Accord. In collaboration with leading global biopharmaceutical companies such as Accord, Abbott, Eurofarma, and KGbio, Henlius has proactively established a global commercial layout for HANQUYOU. Looking ahead, Henlius will continue to strengthen its collaborations with global partners to accelerate the global launch of more high-quality medicines, benefiting more patients worldwide.
About Henlius
联系方式
媒体:PR@Henlius.com
投资者:IR@Henlius.com


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