Mar 20, 2026｜2026
Henlius Reports 2025 Results: Sustained Growth in Both Revenue and Profit, Advancing Innovation Validation and Global Operations
Shanghai, China, March 20, 2026 — Henlius (2696.HK) today announced its annual results for the year ended December 31, 2025. During the reporting period, the Company recorded revenue of RMB 6.6666 billion, representing a year-on-year increase of 16.5%, and net profit of RMB 0.8270 billion. Total R&D investment reached RMB 2.4919 billion, an increase of 35.4%. Amid continued investment in innovation, pre-R&D profit grew to RMB 2.3425 billion, up 26.2% year-on-year. This marks the third consecutive year of profitability and sustained growth of revenue since the Company first achieved full-year profitability in 2023, demonstrating resilient and sustainable profitability, alongside high-quality growth.
In 2025, Henlius continued to strengthen its global growth momentum, with global product revenue reaching RMB 5.7746 billion, up 17.0% year-on-year. Driven by sustained ex-China revenue growth from its core products—serplulimab (trade name: Hetronifly® in Europe) and HANQUYOU (trastuzumab, trade name: HERCESSI™ in the U.S., Zercepac® in Europe)—as well as the accelerating realisation of licensing payments from strategic partnerships, the Company’s ex-China business expanded significantly. Ex-China product revenue exceeded RMB 200 million in 2025, doubling year-on-year, while ex-China product profit increased to RMB 93.9 million. To date, Henlius has achieved approval for 10 products across 60 countries and regions worldwide, including 7 products approved in China, 4 products approved by the U.S. FDA, and 4 products authorized by the European Commission (EC), benefiting more than one million patients globally.
Dr. Jason Zhu, Executive Director and Chief Executive Officer of Henlius, commented: “2025 marked not only a pivotal year for Henlius as we advanced into the era of Globalisation 2.0, but also a year in which our innovation pipeline began to deliver meaningful progress. With continued growth in our ex-China business and ongoing pipeline breakthroughs, we remain firmly committed to a first-principles approach to biopharmaceutical innovation—focusing on deeply understanding and addressing fundamental clinical needs. Looking ahead, Henlius will continue to leverage its integrated platform and global operating capabilities to bring more biologics with quality to patients worldwide, delivering on our long-term commitment to patients through robust innovation.”
Product Revenue Reaches New High, Driven by a Synergistic Commercial Portfolio
In 2025, the synergistic contribution from Henlius' innovative biologics and biosimilars drove total product revenue to a new high.
The Company’s flagship product, serplulimab (trade name: Hetronifly® in Europe), continued to deliver global commercial momentum. During the reporting period, it recorded global sales revenue of RMB 1.4926 billion, representing a year-on-year increase of 13.7%. It received approvals in 2025 in Europe and multiple emerging markets for first-line treatment of extensive-stage SCLC (ES-SCLC), as well as in Indonesia and Thailand for squamous non-small cell lung cancer (sqNSCLC). It has also been included in public reimbursement systems in seven EU countries, including Germany, Italy, and Spain. To date, serplulimab has been approved in over 40 countries and regions worldwide, with continued progress in lung and gastrointestinal cancers, including the potential to set multiple new cancer treatment standards. As the first anti–PD-1 mAb approved globally for first-line treatment of small cell lung cancer, serplulimab is also the first perioperative gastric cancer treatment globally to replace adjuvant chemotherapy with immunotherapy monotherapy. In addition, its international multi-centre phase 3 trial for first-line treatment of metastatic colorectal cancer (mCRC) has completed patient enrolment, with the potential to become the first immunotherapy for first-line treatment of microsatellite stable (MSS) mCRC. With its global commercial potential and differentiated clinical value continuing to expand, Henlius aims to position serplulimab as the next China-developed innovative biologic to surpass RMB 10 billion in annual global sales.
Focusing on broader clinical needs, clinical development and regulatory progress for serplulimab advance with full acceleration across China, the European Union, the United States, Japan, and other emerging markets. In China, the product has been granted Breakthrough Therapy Designation by the National Medical Products Administration for perioperative treatment of gastric cancer. The corresponding marketing application has been accepted and granted priority review, with approval anticipated in the first half of 2026. In parallel, a New Drug Application (NDA) for limited-stage SCLC (LS-SCLC) is planned for submission in China in 2026. In the EU, additional indications—including squamous and non-squamous NSCLC and esophageal squamous cell carcinoma (ESCC)—are expected to receive approval in 2026. In the United States, the bridging study for first-line ES-SCLC has completed enrolment, with a Biologics License Application (BLA) submission planned for 2026.
In 2025, Henlius’ breast cancer franchise maintained strong growth momentum. During the reporting period, global sales revenue from breast cancer products reached RMB 3.2675 billion. Through a combination of in-house R&D and strategic collaborations, the Company has established a comprehensive, end-to-end global treatment portfolio for breast cancer. Its core product HANQUYOU (trastuzumab, trade name: HERCESSI™ in the U.S., Zercepac® in Europe) achieved global sales revenue of RMB 2.9645 billion, up 5.5% year-on-year. To date, HANQUYOU has been approved in more than 50 countries and regions and has been included in reimbursement systems across multiple markets, including China, the United Kingdom, France, and Germany. HANNAIJIA (neratinib) generated sales revenue of RMB 0.3012 billion, representing a year-on-year increase of 564.2%, further strengthening its position as a leading brand in extended adjuvant therapy for HER2-positive early-stage breast cancer. The innovative CDK4/6 inhibitor FUTUONING (fovinaciclib) achieved its first prescriptions in the second half of 2025 and was included in the updated National Reimbursement Drug List. HLX11 (pertuzumab) received approval from the U.S. FDA in the second half of 2025 under the brand name POHERDY®, becoming the first and only1 biosimilar of pertuzumab approved in the U.S. market. In the EU, HLX11 has also received a positive opinion from the European Medicines Agency (EMA), with marketing appliacations submitted in both China and Canada. In this therapeutic area, the Company continues to expand a comprehensive innovation portfolio, including novel endocrine therapy, novel epitope anti-HER2 mAb, HER2-targeted ADC, KAT6A/B oral small-molecule inhibitor, subcutaneous formulation of pertuzumab and trastuzumab, dual-epitope HER2 ADC, and LIV-1 ADC.
Meanwhile, mature commercialized products continued to generate stable cash flow. HANBEITAI (bevacizumab) generated sales revenue of RMB 0.3564 billion, up 80.8%. Pursuant to agreements with its partners, the Company generated RMB 0.6117 billion in sales and licensing revenue from HANLIKANG (rituximab), up 11.1% year-on-year; HANDAYUAN (adalimumab) achieved sales and licensing revenue of RMB 59.2 million, up 47.6%. In the second half of 2025, two dosage strengths of HLX14 (denosumab) were approved in the United States, the European Union, and the UK under the trade names BILDYOS® (60 mg/mL) and BILPREVDA® (120 mg/1.7 mL), respectively, and were recently approved in Canada under the trade names BILDYOS® and TUZEMTY®, becoming the first “China-developed” denosumab to approved in ex-China markets. Currently, the two dosage strengths of HLX14 have been commercially launched in the United States as well as in Germany, Spain and the UK, generating sales revenue of RMB 9.8 million during the reporting period.
Accelerating Global Expansion and Advancing Innovation Pipeline
In 2025, Henlius accelerated its Globalisation 2.0 strategy. During the reporting period, the Company continued to expand its footprint in international regulatory filings and commercial collaborations. It secured 27 Investigational New Drug (IND) approvals and 28 new marketing approvals worldwide, covering more than 60 countries and regions across China, the United States, Europe, Japan, and Canada. At the same time, clinical studies are being actively advanced in nearly 30 countries and regions, further accelerating the global development of its pipeline. Meanwhile, Henlius continued to expand its global partnership network. During the reporting period, the Company entered into collaborations with leading international partners including Abbott, Eisai and Lotus regarding rights to serplulimab. In addition, Henlius established licensing partnerships with Dr. Reddy’s and Sandoz for HLX15 (daratumumab) and HLX13 (ipilimumab), respectively.
As a key innovative asset of the Company, dulpatatug (HLX22)2, a novel epitope anti-HER2 mAb, continues to make steady progress in its international multi-centre phase 3 clinical trial for the treatment of HER2-positive gastric cancer in a head-to-head comparison with standard first-line therapy. The study has initiated first patient dosing across multiple countries and regions, including China, the United States, Europe, Japan, Australia, South Korea, and Latin America. Two years of follow-up results from its phase 2 study in gastric cancer were presented at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting, demonstrating durable efficacy and favourable outcomes compared to historical benchmarks, with an approximately 80% reduction in the risk of disease progression or death in the overall population. Beyond gastric cancer, dulpatatug is being further developed across additional indications, including breast cancer. Its phase 2 study in HER2-low breast cancer has completed patient enrolment, while a phase 2/3 study evaluating dulpatatug in combination with the HER2-targeted ADC HLX87 for first-line treatment of HER2-positive breast cancer has completed first patient dosing.
HLX43, a PD-L1-targeted ADC with potential best-in-class (BIC) characteristics and broad anti-tumour activity across multiple tumour types, continues to demonstrate its “pipeline-in-a-pill” potential. Early clinical data from its first-in-human study, along with multiple proof-of-concept results across solid tumours, have been presented at several international scientific conferences, showing a favourable efficacy and safety profile. Notably, in non-small cell lung cancer (NSCLC), HLX43 has demonstrated activity without the need for biomarker-based patient selection, suggesting potential applicability across a broad patient population. In addition to NSCLC, encouraging signals have also been observed in gynecological tumours, esophageal squamous cell carcinoma (ESCC), and other solid tumours. Beyond monotherapy, the Company is actively exploring combination strategies of HLX43 with anti-EGFR mAb pimurutamab (HLX07) and serplulimab, aiming to further expand its clinical potential. In 2026, Henlius plans to accelerate proof-of-concept studies across a broader range of solid tumours while advancing multiple global pivotal trials efficiently.
In 2025, Henlius continued to strengthen its platform-based innovation capabilities, establishing a multi-dimensional technology ecosystem. This includes a next-generation immuno-oncology (IO) platform, the proprietary Hanjugator™ ADC platform, a tri-specific T-cell engager (TCE) platform, and HAI Club—an AI-driven, integrated platform for early-stage antibody discovery and development. During the reporting period, multiple candidates—including HLX37 (PD-L1 × VEGF bispecific antibody), HLX97 (KAT6A/B small-molecule inhibitor), HLX3901 (DLL3 × DLL3 × CD3 × CD28 tetra-specific TCE), and HLX316 (B7-H3 sialidase fusion protein)—received Investigational New Drug (IND) approvals. Meanwhile, the Company continues to advance a number of promising pipeline assets, including HLX3902 (STEAP1 × CD3 × CD28 tri-specific TCE), HLX48 (EGFR × c-MET bispecific ADC), HLX49 (HER2 dual-epitope ADC), and HLX109 (IL-1R3 mAb), further enriching its globally competitive innovation portfolio.
As a critical foundation for its Globalisation 2.0 strategy, Henlius continued to enhance its manufacturing and quality systems. The Company's Xuhui Site, Songjiang Site I, and Songjiang Site II have a total installed capacity of 84,000 litres. To date, Henlius has completed more than 1,300 GMP commercial production batches, enabling stable and continuous global supply of its products. The Company’s commercial manufacturing facilities and associated quality management systems have successfully undergone nearly 100 on-site inspections and audits conducted by regulatory authorities and international partners worldwide, with no critical findings and a 100% pass rate. Henlius has obtained GMP certifications from China, the European Union, the United States, and multiple member countries of the Pharmaceutical Inspection Co-operation Scheme (PIC/S), as well as three ISO certifications, including ISO 9001, ISO 14001, and ISO 45001. During the reporting period, the Company further strengthened its global commercial supply capabilities. Four products—serplulimab, HANQUYOU, and two dosage strengths of denosumab (HLX14)—achieved their ex-China shipments, covering eight countries, including the United States, the UK, Germany, Spain, and India. In total, more than 30 ex-China shipments were completed during the year. Meanwhile, Henlius continued to advance its international manufacturing and quality infrastructure. In 2025, HLX14 marked its first commercial shipment to Europe, with the Company completing the full regulatory approval process in its role as Marketing Authorization Holder (MAH) for the first time. In Japan, the supporting quality system for MAH operations has also been successfully established.
Patient-Centric Approach, Advancing a China-Rooted Global Biopharma Model
Looking ahead, Henlius remains committed to its patient-centric mission. Leveraging its solid commercial foundation, continuously evolving innovation engine, and increasingly integrated global operations, the Company aims to bring more biologics with quality to patients worldwide. Guided by its 2030 vision, Henlius will continue to advance its global strategy and further evolve into a globally operating biopharmaceutical company headquartered in China. Looking forward, Henlius targets achieving more than 20 product approvals globally, including over 15 in the United States and Europe, further strengthening its position as an internationally competitive and globally influential biopharmaceutical company.
References
1. U.S. FDA official website, accessed on March 20, 2026
2. The drug’s generic name is currently in pINN status
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Privacy Policy
Introduction
Shanghai Henlius Biotech, Inc., and, where applicable, its affiliates and subsidiaries (collectively, “we” , “us” or “our”) attach great importance to the protection of your privacy and personal information. This Privacy Notice (this “Policy”) is formulated in accordance with applicable PRC laws and regulations governing the protection of personal information in the People’s Republic of China (“PRC”).
This Policy applies when: (1) you browse or use our website and other online resources (such as our WeChat official accounts); (2) subscribe to our news or announcements; or (3) contact us through the contact details or other interactive features made available on our website, or otherwise interact with us through our website.. The purpose of this Policy is to explain how and why we process your personal information, the types of personal information involved, applicable retention periods, your rights, and the measures we take to protect personal information. Please read this Policy carefully to ensure that you fully understand its content.
In certain business scenarios, we may provide additional explanations regarding the processing of your personal information through separate agreements, privacy statements, or personal information notices. In the event of any inconsistency, such documents shall prevail. For example, where a recruitment function is provided through a third-party platform or service, the relevant third party privacy policy or notice may also apply.
For the purposes of this Policy, “personal information” refers to all kinds of information related to identified or identifiable natural persons, excluding anonymized information.
We collect, use, store, transfer and otherwise process personal information in strict compliance with applicable PRC laws and regulations of the People’s Republic of China.
Our website may contain links to third party websites for your convenience. We do not control, and are not responsible for, the privacy practices of such third parties. We encourage you to review their privacy policies before using those websites.
If you have any questions or concerns regarding this Policy or our processing of personal information, please contact us using the details provided below.
This Policy will help you understand:
I. How we collect your personal information
II. How we use your personal information
III. How we entrust, share, transfer and publicly disclose your personal information
IV. Cross border transfer of personal information
V. How we store your personal information
VI. Security measures
VII. Your rights
VIII. Personal information of minors
IX. Updates to this Policy
X. How to contact us
I. How do we collect your personal information?
In addition to our employees, we may process personal information of the following persons:
• Visitors and users of our website;
• Healthcare Professionals;
• Investigators of clinical trial institutions and personnel of contract research organizations in clinical trials;
• Subjects of clinical trials and their relatives;
• Consumers/patients and their relatives using our products or services;
• Staff of business partners (including vendors, distributors, partners, etc.); and
• Our applicants.
We may process personal information of website visitors and individuals who contact or interact with us through our website or other online resources. Depending on the relevant page, function, or interaction, separate privacy notices, consents, platform privacy policies, contracts, or other notices may apply.
Based on the context in which you interact with us, we may collect personal information by the following means and on the legal bases permitted by applicable PRC laws and regulations, including your consent, the necessity for entering into or performing a contract, compliance with legal obligations, protection of life, health or property, public health needs, or other circumstances permitted by law:
• Your personal information provided to us voluntarily
When you subscribe to our news or announcements, contact us through the contact details or other interactive features made available on our website, a third-party platform or service linked or referred to on our website, or otherwise communicate with us in relation to our website, we may collect the personal information that you voluntarily provide, such as your name, contact details, organization, and the content of your inquiry or request, depending on the relevant page or function.
• Personal information collected by us independently through our website and other online channels
When you visit our website, most of our services do not require any registration, and you can visit our website without telling us who you are. However, some pages or functions may require you to provide certain personal information. If you choose not provide such information as we request, you may not be able to access certain content or functions or we may not be able to respond to your inquiry, request or subscription. Please refer to the relevant page or notice for further details about the categories of personal information collected in a specific scenario.
• Personal information we collect from vendors or business partners
In the course of our daily business operations, we may collect personal information from our vendors or business partners. We require our vendors and business partners to comply with the requirements of the personal information protection laws and regulations of the PRC and to lawfully provide us with personal information. If you are an employee or representative of one of our vendors or business partners, we may collect personal information such as your name and contact details for the purpose of establishing business contacts and cooperations.
• Personal information we collect from publicly available sources
We may collect personal information of medical and healthcare professionals from such publicy available sources, such as the official websites of medical institutions and the official websites of competent government departments, and process such information within a reasonable scope and for lawful purposes. For example, for the purpose of lawful academic or professional interaction with healthcare professionals, we may collect the name, gender, employer, position, practitioner registration information, academic title, degree, educational background, specialty expertise, and profile information, where such information has been lawfully made public.
Our website may include links, contact details, QR codes, or references to third-party platforms or services. Where you choose to interact with us through such third-party platforms or services, the relevant third party may also process your personal information in accordance with its own privacy policy and applicable law, and we encourage you to review such policy before submitting your information.
II. How do we use your personal information?
We may use your personal information for the following purposes:
• Operating, maintaining and improving our website and other online resource;
• Researching, developing, providing and continuously improving our products and services;
• Conducting and managing daily business;
• Academic interaction with healthcare professionals;
• Responding to your inquiries, requests, or communications sent through our website or the contact details made available on our website;
• Providing subscription services for our news, announcements, or investor-related updates;
• Managing and maintaining our relationship and communications with business contacts who reach us through our website;
• Recruiting and human resource management;
• Internal compliance management，audit，record-keeping; and
• Complying with applicable PRC laws and regulations, for example, monitoring and reporting adverse events for purposes of performing drug quality management responsibilities, providing medical information and dealing with product complaints, etc..
We will process personal information only to the extent necessary for the relevant purpose. Where required by applicable law, we will obtain your consent or separate consent before processing your personal information or sensitive personal information. Where a third-party platform or service is used in connection with a particular function, the relevant third party may process your personal information in accordance with its own privacy policy and applicable law.
III. How do we entrust, share, transfer and publicly disclose your personal information?
1. Entrustment
We may entrust our business partners with the processing of your personal information for the purpose(s) described in this Policy. We will enter into appropriate confidentiality, data processing and security agreements with such entrusted parties and require them to process personal information in accordance with our instructions , this Policy and applicable PRC laws and regulations.
2. Sharing and public disclosure
For the purpose(s) described in this Policy, we will share or publicly disclose your personal information only where permitted by applicable PRC laws and regulations and, where required, after obtaining your consent or separate consent. Such circumstances may include:
• Sharing your personal information among our affiliates and subsidiaries where necessary for legitimate business, management, compliance, or operational purposes;
• Sharing your personal information with vendors or business partners (such as conference service providers, travel service providers, data service providers, banking or insurance institutions, other professional service organizations, to the extent necessary for the relevant purpose); and
• Disclosing your personal information to the extent that it is permitted or required by applicable PRC laws and regulations or for the purpose of assisting with investigations by judicial, regulatory or law enforcement authorities.
• other circumstances permitted by applicable PRC laws and regulations.
If you submit your information through or in connection with a third-party platform or service referred to on our website, the relevant third party may independently process your personal information in accordance with its own privacy policy and applicable law.
3. Transfer
We will not transfer your personal information to any other company, entity or individual unless otherwise permitted by applicable law and, where required, after obtaining your consent. Further, in the event of a merger, acquisition, insolvency, reorganization, division, dissolution, bankruptcy, or similar transaction, we will require the new processor of your personal information to continue to be bound by this Policy or we will require the new processor to obtain your consent again.
IV.How do we provide your personal information across borders?
In principle, personal information that we collect and generate in the course of our operations within the territory of the PRC will be stored within the PRC. In certain circumstances, it may be necessary for us to provide your personal information to recipients outside the PRC in connection with our business operations, website functions, or communications, where permitted by applicable PRC laws and regulations. As required by applicable laws and regulations regarding the protection of personal information, we will provide you with the required notice and obtain your separate consent before providing your personal information across any border, unless otherwise permitted by law. We will use lawful cross-border transfer mechanisms to transfer your personal information oversea and will take necessary measures to ensure that the oversea recipients provide a level of protection required by applicable PRC laws and regulations.
You may obtain more information about cross-border transfers of personal information and oversea recipients through the contact methods referred to in this Policy.
V. How do we store your personal information?
We will retain your personal information for the minimum period necessary to achieve the purposes described in this Policy ,unless a longer retention period is required or permitted by applicable PRC laws and regulations. Upon expiration of the applicable retention period, we will promptly delete or anonymize your personal information in accordance with applicable PRC laws and regulations. Our criteria for determining the period for which personal information shall be retained include:
• Applicable laws, regulations and other relevant requirements;
• The period of time needed for us to provide services, maintain business relations or interact with you; and
• The period of time needed for us to perform relevant agreements or fulfil the purposes described in this Policy.
VI. What security measures do we take to protect your personal information?
In accordance with applicable PRC laws, regulations, and the requirements of relevant national standards, we take reasonable and appropriate security and precautionary measures to protect the personal information we process against unauthorized access, public disclosure, use, modification, destruction or loss of data. However, you are also responsible for taking appropriate measures to protect the security of the devices, systems, and networks you use when accessing our website or communicating with us.
VII. Your rights
In accordance with the requirements of the applicable PRC laws and regulations, you may have the following rights in respect of your personal information:
• To know about and make decisions regarding the processing of your personal information;
• To access or copy your personal information;
• To correct or supplement your personal information;
• To delete your personal information;
• To request for explanation of rules regarding processing of personal information; and
• To change the scope of your consent or revoke your consent , where processing is based on your consent.
If you wish to exercise your rights with respect to personal information, you may contact us through the contact information listed in this Policy and we will respond to any request in accordance with applicable relevant laws and regulations. When you exercise the above rights, we may verify your identity to safeguard the security of your personal information. Subject to applicable PRC laws and regulations, there may be circumstances where we are unable to respond to all or part of your request.
VIII. How do we process the personal information of minors?
For the purposes of this Policy and in accordance with applicable PRC laws and regulations, our products, websites and services are not targeted at minors under the age of 14. Minors under the age of 14 should not provide personal information to us without the consent of a parent or legal guardian.
If a minor's personal information is collected with the consent of a parent or legal guardian, we will process the information only when permitted by law, with the express consent of the parent or legal guardian, or necessary for the protection of the minor. If we discover that we have collected personal information without obtaining verifiable prior consent of a parent or legal guardian, we will seek to delete the data as soon as possible.
IX. Updates of the Policy
We may revise our Privacy Policy from time to time. We will post the updated version on our website and update the “Last Updated” date above or below this Policy.
Last updated: March 30, 2026.
X. How to contact us?
If you have any questions, comments or suggestions concerning this Policy, or any questions or concerns about our processing of your personal information, you may contact us in the following ways:
Address: 11/F, B8 Building, No.188 Yizhou Rd, Xuhui District, Shanghai
Tel.: 021- 33395800
Postal Code: 200233
Email: PR@nyyfx.com
Cookies Policy
When you visit our website, we may place small data files known as “cookies” on your device. Cookies enable our website to recognize your browser and help us understand how visitors use the site.
Cookies and similar technologies used on this website may collect online identifiers, device information, browser information, IP address, and information about how you interact with the website. In certain circumstances, such information may constitute personal information or may be associated with you under applicable PRC laws and regulations. Information collected through cookies is used for purposes such as ensuring website operation, maintaining security, analyzing traffic and performance, remembering user preferences, and improving website content and user experience.
You may choose to accept or decline cookies by adjusting your browser settings or through any cookie banner or preference center made available on our website, if applicable. Please note that disabling cookies may affect the functionality of certain parts of the website.
For more information about how we process personal information, please refer to our Privacy Notice.
Some cookies may be provided by third parties. Where third-party cookies or similar technologies are used, such third parties may process the relevant information in accordance with their own privacy policies and applicable PRC laws and regulations.
Accessibility
Shanghai Henlius Biotech, Inc. (“Henlius”) is committed to improving the accessibility and user friendliness of its website for all visitors.
We strive to ensure that the content on our website can be accessed and used by individuals with diverse needs, including those who rely on assistive technologies. As our website continues to evolve, we recognize that accessibility is an ongoing effort, and we are continuously working to improve usability and accessibility across our digital platforms.
If you experience difficulty accessing any part of our website, or have suggestions on how we can enhance accessibility, we welcome your feedback. To help us respond effectively, please include the specific webpage address (URL) and a brief description of the issue encountered.
Contact us:
Email: PR@nyyfx.com
(Please include “Website Accessibility” in the subject line)
Henlius will make reasonable efforts to review accessibility-related feedback and improve the overall online experience for all users. While we strive to improve accessibility, we do not guarantee that every page or feature will be fully accessible to every user in all circumstances.
Terms of Use
This website (http://www.nyyfx.com/) is developed and operated by Shanghai Henlius Biotech, Inc. (“Henlius”). Please read these Terms of Use carefully before accessing or using this website. By accessing, browsing or using this website, you acknowledge that you have read, understood and agreed to be bound by these Terms of Use and applicable PRC laws and regulations.
Henlius reserves the right to modify or update these Terms of Use at any time. Any updated version will be posted on this website with a revised “Last Updated” date. Please review them periodically for updates.
Prohibited Conduct:
You shall not infringe the lawful rights and interests of Henlius or any third party, nor interfere with or attempt to interfere with the normal operation, security, or integrity of this website by any means. Without limitation, you shall not use this website for any unlawful purpose, attempt unauthorized access to any part of the website or related systems, introduce malicious code, scrape or extract website content through automated means, or otherwise interfere with the website’s operation or security features.
Copyright
All content on this website, including but not limited to text, data, logos, graphics, audio, video and other materials, is owned by Henlius or its respective rights holders, unless otherwise stated. Such content is protected by applicable Chinese and international copyright laws. This website and its content may be accessed and used only for lawful, personal, and non-commercial purposes. Without prior written consent, no entity or individual may copy, reproduce, republish, upload, post, transmit, distribute, modify, create derivative works from, mirror, or otherwise use such content for commercial or public purposes.
Disclaimers
To the fullest extent permitted by applicable PRC laws and regulations, Henlius makes no warranties or representations, express or implied, regarding the content of this website, including but not limited to accuracy, completeness, timeliness or suitability for any particular purpose. Henlius does not undertake any obligation to update the content of this website , except as otherwise required by applicable PRC laws and regulations.
You use this website and any information obtained from it at your own risk. To the fullest extent permitted by applicable PRC laws and regulations, Henlius shall not be liable for any loss or damage arising from the use or inability to use this website, including but not limited to system failures, computer viruses or data loss.
Medical Information
Nothing on this website constitutes medical advice, diagnosisor treatment recommendations. Medical decisions should always be made in consultation with qualified healthcare professionals. Any product-related or disease-related information provided on this website is provided for general informational purposes only and should not be construed as medical advice, diagnosis, or treatment recommendations; any product information is subject to the approved prescribing information and applicable local laws and regulations.
Third Party Websites
This website may contain links to third party websites for convenience. Henlius is not responsible for the content, availability, privacy practices, terms or use of such third-party websites. Access to third party websites is at your own risk.
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Henlius respects your privacy. Please refer to our Privacy Notice for details.
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These Terms of Use shall be governed by the laws of the People’s Republic of China.
Last updated: March 30, 2026
