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    2025 AACR | 复宏汉霖多项最新研究成果入选

    VEGF PDL1 癌症
    04/01
    31

    2025年美国癌症研究协会(AACR)年会将于4月25日-4月30日在美国芝加哥召开。复宏汉霖将在本次大会上报告3项自主研发的最新临床前研究成果,包括一款抗PD-L1和抗VEGF双靶点的双特异性抗体HLX37、一项潜在成为同类最佳的KAT6A/B候选分子,以及一个同类首创具有特异性杀伤作用的ADC技术平台。美国癌症协会(AACR)年会是世界上历史最悠久、最大的科学会议之一,会议关注高质量癌症研究及各方面的创新成果。


    复宏汉霖秉持差异化的创新研发策略,在以抗体技术为核心的创新领域持续推进,构建了约50个分子的多元化管线,致力于加速更多潜在“First-in-Class”和“Best-in-Class”分子进入临床开发阶段。目前管线覆盖单抗、多抗、抗体偶联药物(ADC)、融合蛋白等丰富的药物形式,并持续深化AI等前沿技术和平台赋能,破解临床之需并促进创新成果转化落地。


    本次发布摘要信息如下:




    摘要标题:A novel anti-PD-L1/VEGF bispecific antibody (HLX37) with immune checkpoint inhibition, anti-angiogenic, and antineoplastic activities

    分会场标题:Overcoming Checkpoint Inhibition and Tumor Suppression

    展示形式:摘要及壁报   

    摘要编号:7303 

    展示时间:美国中部时间4月30日(周三)9:00 AM-12:00 PM

    展示地点:第39区,展板#18




    摘要标题:Discovery of a novel antibody-drug conjugate linker-payload with a distinct killing mechanism via prolonged unfolded protein response activation

    分会场标题:Drug Design, Synthesis, and Disposition

    展示形式:摘要及壁报   

    摘要编号:5730

    展示时间:美国中部时间4月29日(周二)2:00 PM-5:00 PM

    展示地点:第25区,展板#1




    摘要标题:Identification of novel KAT6A/B inhibitors with enhanced antitumor activity and reduced hematologic toxicity

    分会场标题:Lead Identification and Optimization

    展示形式:摘要及壁报   

    摘要编号:6976 

    展示时间:美国中部时间4月30日(周三)9:00 AM-12:00 PM

    展示地点:第25区,展板#5

    关于复宏汉霖

    复宏汉霖(2696.HK)是一家国际化的创新生物制药公司,致力于为全球患者提供可负担的高品质生物药,产品覆盖肿瘤、自身免疫疾病、眼科疾病等领域,已有6款产品在中国获批上市,4款产品在国际获批上市,5个上市申请分别获中国药监局、美国FDA和欧盟EMA受理。自2010年成立以来,复宏汉霖已建成一体化生物制药平台,高效及创新的自主核心能力贯穿研发、生产及商业运营全产业链。公司已建立完善高效的全球创新中心,按照国际药品生产质量管理规范(GMP)标准进行生产和质量管控,不断夯实一体化综合生产平台,其中,公司商业化生产基地已相继获得中国、欧盟和美国GMP认证。


    复宏汉霖前瞻性布局了一个多元化、高质量的产品管线,涵盖约50个分子,并全面推进基于自有抗PD-1单抗H药汉斯状®的肿瘤免疫联合疗法。截至目前,公司已获批上市产品包括国内首个生物类似药汉利康®(利妥昔单抗)、自主研发的中美欧三地获批单抗生物类似药汉曲优®(曲妥珠单抗,美国商品名:HERCESSI™,欧洲商品名:Zercepac®)、汉达远®(阿达木单抗)、汉贝泰®(贝伐珠单抗)、全球首个获批一线治疗小细胞肺癌的抗PD-1单抗汉斯状®(斯鲁利单抗,欧洲商品名:Hetronifly®)以及汉奈佳®(奈拉替尼)。公司亦同步就19个产品在全球范围内开展30多项临床试验,对外授权全面覆盖欧美主流生物药市场和众多新兴市场。



    Henlius to Present Three Preclinical Studies at AACR 2025


    The American Association for Cancer Research 2025 Annual Meeting (AACR 2025) is set to take place from April 25 to April 30 in Chicago, the United States. Henlius will share three latest preclinical research results from its pipeline programs. The results to be presented include the novel anti-PD-L1/VEGF bispecific antibody HLX37, a novel KAT6A/B inhibitors with best-in-class potential, and a first-in-class ADC linker-payload featuring a highly differentiated killing mechanism. AACR is the oldest and largest scientific organization in the world focused on every aspect of high-quality, innovative cancer research.

     

    Henlius has maintained a differentiated innovation strategy and is committed to drive innovation in antibody technology to accelerate the development of potential "First-in-Class" and "Best-in-Class" molecules into clinical stages. The company has built a pipeline of about 50 molecules, including monoclonal antibodies (mAbs), polyclonal antibodies (pAbs), antibody-drug conjugates (ADCs), and fusion proteins. Meanwhile, Henlius also leverages cutting-edge technologies such as AI to address unmet clinical needs and enhance the translation of innovative achievements.

     

    Details of the abstract are as follows:


    Title: A novel anti-PD-L1/VEGF bispecific antibody (HLX37) with immune checkpoint inhibition, anti-angiogenic, and antineoplastic activities

    Session Title: Overcoming Checkpoint Inhibition and Tumor Suppression

    Form: Abstract and poster

    Abstract Number: 7303

    Date and Time: April 30, 2025, 9:00 AM-12:00 PM CST

    Location: Poster Section 39, Board #18

    Title: Discovery of a novel antibody-drug conjugate linker-payload with a distinct killing mechanism via prolonged unfolded protein response activation

    Session Title: Drug Design, Synthesis, and Disposition

    Form: Abstract and poster

    Abstract Number: 5730

    Date and Time: April 29, 2025, 2:00 PM-5:00 PM CST

    Location: Poster Section 25, Board #1

    Title: Identification of novel KAT6A/B inhibitors with enhanced antitumor activity and reduced hematologic toxicity

    Session Title: Lead Identification and Optimization

    Form: Abstract and poster

    Abstract Number: 6976

    Date and Time: April 30, 2025, 9:00 AM-12:00 PM CST

    Location: Poster Section 25, Board #5

    About Henlius

    Henlius (2696.HK) is a global biopharmaceutical company with the vision to offer high-quality, affordable and innovative biologic medicines for patients worldwide with a focus on oncology, autoimmune diseases and ophthalmic diseases. Up to date, 6 products have been launched in China, 4 have been approved for marketing in overseas markets, and 5 marketing applications have been accepted for review in China, the U.S. and the EU, respectively. Since its inception in 2010, Henlius has built an integrated biopharmaceutical platform with core capabilities of high-efficiency and innovation embedded throughout the whole product life cycle including R&D, manufacturing and commercialization. It has established global innovation centre and Shanghai-based commercial manufacturing facilities certificated by China, the EU and U.S. GMP.


    Henlius has pro-actively built a diversified and high-quality product pipeline covering about 50 molecules and has continued to explore immuno-oncology combination therapies with proprietary HANSIZHUANG (anti-PD-1 mAb) as the backbone. To date, the company's launched products include HANLIKANG (rituximab), the first China-developed biosimilar, HANQUYOU (trastuzumab, trade name: HERCESSI™ in the U.S., Zercepac® in Europe), a China-developed mAb biosimilar approved in China, Europe and U.S., HANDAYUAN (adalimumab), HANBEITAI (bevacizumab), HANSIZHUANG (serplulimab, trade name: Hetronifly® in Europe), the world’s first anti-PD-1 mAb for the first-line treatment of SCLC, and HANNAIJIA (neratinib). What’s more, Henlius has conducted over 30 clinical studies for 19 products, expanding its presence in major markets as well as emerging markets.


    联系方式

    媒体:PR@Henlius.com

    投资者:IR@Henlius.com



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