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    May 13, 2026|2026
    Henlius' potential BIC oral KAT6A/B inhibitor HLX97 completes first patient dosing in Phase 1, aiming to overcome endocrine therapy resistance in breast cancer

    Shanghai, China, May 13, 2026 — Shanghai Henlius Biotech, Inc. (2696.HK) announced that the first patient has been dosed in a Phase 1 clinical trial of HLX97, a novel oral lysine acetyltransferase 6A/B (KAT6A/B) small molecule inhibitor, in patients with advanced or metastatic solid tumors in China. Previously, the Investigational New Drug (IND) application for HLX97 in advanced/metastatic solid tumors was approved by the China National Medical Products Administration (NMPA).


    Breast cancer is the second most common cancer worldwide and the most common malignant tumor among women, and it is also a leading cause of cancer-related death in women. ER-positive (ER+) breast cancer is the most prevalent subtype, accounting for approximately 70% of all cases.1 While endocrine therapies—such as estrogen suppression and direct targeting of the estrogen receptor—have become the cornerstone of treatment and significantly reduced recurrence and mortality, both primary and acquired resistance remain major clinical challenges.


    KAT6A (Lysine Acetyltransferase 6A) and its paralog KAT6B (Lysine Acetyltransferase 6B) are members of the MYST family of histone acetyltransferases (HATs) and play key roles in tumorigenesis, disease progression, and the development of drug resistance across multiple cancer types. Preclinical and clinical studies have shown that amplification and/or overexpression of the KAT6A gene is closely associated with endocrine resistance in heavily pretreated patients with ER+/HER2- metastatic breast cancer. In addition, aberrant expression of KAT6A/B has been observed in a range of solid tumors, including ovarian, cervical, colorectal, prostate, lung cancers, and gliomas, suggesting broad therapeutic potential for KAT6A/B inhibitors across tumor types.2-4 Given that amplification and/or overexpression of the KAT6A gene in breast cancer has been shown to be closely associated with the development of endocrine resistance, targeting KAT6A/B activity may represent a promising strategy to overcome endocrine therapy resistance in breast cancer.5-6


    HLX97 is a novel oral KAT6A/B inhibitor with best-in-class potential. By selectively inhibiting KAT6A/B activity, HLX97 is designed to regulate tumor cell proliferation and induce apoptosis. It demonstrates high selectivity and favorable pharmacokinetic properties characterized by rapid onset and clearance, aiming to maximize antitumor activity while minimizing hematological toxicity. Preclinical studies have shown that HLX97 effectively inhibits KAT6A/B activity and exhibits strong antitumor efficacy with a favorable safety profile. In animal models, HLX97 demonstrated significant efficacy in ER-positive breast cancer as well as in human-derived xenograft models resistant to both fulvestrant and palbociclib (a CDK4/6 inhibitor), with good overall tolerability.


    Henlius has built a comprehensive pipeline covering the full continuum of breast cancer care through internal innovation and strategic collaborations. Its marketed products include HANQUYOU (trade name: HERCESSI in the U.S., Zercepac® in Europe), a trastuzumab biosimilar approved in over 50 countries and regions including China, the U.S., and Europe; POHERDY®, the first pertuzumab biosimilar approved in the U.S.; HANNAIJIA (neratinib), an extended adjuvant therapy for early-stage breast cancer, and CDK4/6 inhibitor FUTUONING (fovinaciclib). Meanwhile, Henlius is advancing next-generation molecules such as novel epitope anti-HER2 antibody HLX22, oral selective estrogen receptor modulator (SERM) lasofoxifene (HLX78), KAT6A/B inhibitor HLX97, LIV-1-targeting ADC HLX41, HER2×HER2 bispecific epitope ADC HLX49 and HER2 ADC HLX87 through its robust innovation platforms and collaborative R&D. Building on this foundation, Henlius remains committed to advancing monotherapies and combination regimens across all breast cancer subtypes, enhancing therapeutic value through strengthened pipeline synergies.


    Moving forward, Henlius will continue to focus on unmet clinical needs by fully leveraging its integrated platform advantages in antibody-based drugs, expanding disease areas, accelerating the development of differentiated molecules, and bringing more high-quality, affordable innovative therapies to patients worldwide.


    About HLX97-FIH101

    This study is a multicenter, open-label phase 1 clinical trial designed to evaluate the safety, tolerability, pharmacokinetic (“PK”) characteristics, and preliminary antitumor activity of HLX97 in patients with advanced or metastatic solid tumors. The study consists of two parts: Part 1 is the dose‑escalation phase, which includes monotherapy dose escalation (Part 1A) and combination therapy dose escalation (Part 1B); Part 2 is the dose‑expansion phase. Part 1A, the monotherapy dose‑escalation phase, will be conducted in patients with advanced/metastatic solid tumors and will include five dose levels ranging from 1.0 mg to 15.0 mg. HLX97 will be administered orally from Day1 to Day28 of each cycle, once a day, for 4 weeks each cycle. Part 1B, the combination therapy dose‑escalation phase, will explore 2 to 3 dose levels of HLX97 in combination with fulvestrant in patients with HR‑positive, HER2‑negative locally advanced or metastatic breast cancer. Part 2 will be conducted in patients with HR‑positive, HER2‑negative locally advanced or metastatic breast cancer and will include 3 treatment groups: two groups receiving different doses of HLX97 in combination with fulvestrant, and one group receiving fulvestrant monotherapy. The primary endpoints of Part 1 are to evaluate the incidence of dose‑limiting toxicities (DLT) and to determine the maximum tolerated dose (MTD) of HLX97 as monotherapy and in combination with fulvestrant. The primary endpoints of Part 2 are the objective response rate (ORR) and progression‑free survival (PFS) as assessed by the investigator according to RECIST version 1.1, as well as the recommended Phase 2 dose (RP2D) of HLX97 in combination with fulvestrant. Secondary endpoints include the safety of HLX97 as monotherapy and in combination, PK parameters, additional efficacy endpoints (such as duration of response (DOR), disease control rate (DCR), and overall survival (OS)), and exploratory pharmacodynamic and predictive biomarker analyses.


    References

    1. Nolan E, et al. Deciphering breast cancer: from biology to the clinic. Cell. 2023;186(8):1708-1728.

    2. Chen J, et al. Mutations of Chromatin Structure Regulating Genes in Human Malignancies. Curr Protein Pept. Sci. 2016;17(5):411-437.

    3. Partynska A, et al. The Expression of Histone Acetyltransferase KAT6A in Non-small Cell Lung Cancer. Anticancer Res. 2022;42(12):5731-5741.

    4. Lv D, et al. Histone Acetyltransferase KAT6A Upregulates PI3K/AKT Signaling through TRIM24 Binding. Cancer Res. 2017;77(22):6190-6201.

    5. Sharma S, et al. Discovery of a highly potent, selective, orally bioavailable inhibitor of KAT6A/B histone acetyltransferases with efficacy against KAT6A-high ER+ breast cancer. Cell Chem Biol. 2023;30(10):1191-1210.e20.

    6. Yu L, et al. Identification of MYST3 as a novel epigenetic activator of ERα frequently amplified in breast cancer. Oncogene. 2017;36(20):2910-2918.


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    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”).

     

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    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

     

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    In addition to our employees, we may process personal information of the following persons:

     

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    • Providing subscription services for our news, announcements, or investor-related updates;

     

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    • 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.

     

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    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.

     

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    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.

     

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    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.

     

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    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:

     

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    • 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.

     

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    Last updated: March 30, 2026