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81.
公开(公告)号:US20190127480A1
公开(公告)日:2019-05-02
申请号:US16205917
申请日:2018-11-30
发明人: Jessica R. Kirshner , Alison Crawford , Gavin Thurston , Eric Smith , Lauric Harber , Drew Dudgeon , Ashique Rafique
摘要: The present invention provides antibodies that bind to prostate-specific membrane antigen (PSMA), bispecific antibodies that bind to PSMA and CD3, and methods of using the same. According to certain embodiments, the antibodies of the invention bind human PSMA with high affinity and bind CD3 to induce human T cell proliferation. The invention includes antibodies that bind PSMA and CD3 and induce T cell-mediated killing of PSMA-expressing tumor cells. According to certain embodiments, the present invention provides bispecific antigen-binding molecules comprising a first antigen-binding domain that specifically binds human CD3, and a second antigen-binding molecule that specifically binds human PSMA. In certain embodiments, the bispecific antigen-binding molecules of the present invention are capable of inhibiting the growth of prostate tumors expressing PSMA. The antibodies and bispecific antigen-binding molecules of the invention are useful for the treatment of diseases and disorders in which an upregulated or induced targeted immune response is desired and/or therapeutically beneficial. For example, the antibodies of the invention are useful for the treatment of various cancers.
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公开(公告)号:US09982013B2
公开(公告)日:2018-05-29
申请号:US15058026
申请日:2016-03-01
发明人: Samuel Davis , Eric Smith , Douglas MacDonald , Kara Louise Olson
CPC分类号: C07K1/22 , A61K2039/505 , C07K16/247 , C07K16/248 , C07K16/2809 , C07K16/2866 , C07K16/2887 , C07K16/468 , C07K2317/21 , C07K2317/31 , C07K2317/52 , C07K2317/526 , C07K2317/56 , C07K2317/76
摘要: A bispecific antibody format providing ease of isolation is provided, comprising immunoglobulin heavy chain variable domains that are differentially modified in the CH3 domain, wherein the differential modifications are non-immunogenic or substantially non-immunogenic with respect to the CH3 modifications, and at least one of the modifications results in a differential affinity for the bispecific antibody for an affinity reagent such as Protein A, and the bispecific antibody is isolable from a disrupted cell, from medium, or from a mixture of antibodies based on its affinity for Protein A.
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83.
公开(公告)号:US20180118848A1
公开(公告)日:2018-05-03
申请号:US15713578
申请日:2017-09-22
发明人: Lauric Haber , Eric Smith , Marcus Kelly , Jessica R. Kirshner , Sandra Coetzee , Alison Crawford , Thomas Nittoli , Yashu Liu
IPC分类号: C07K16/30 , G01N33/574 , C07K16/28 , A61K47/68
CPC分类号: C07K16/3092 , A61K39/395 , A61K39/39558 , A61K47/6849 , A61K47/6851 , A61K47/6869 , A61K2039/505 , C07K16/2809 , C07K16/2863 , C07K16/3069 , C07K16/44 , C07K16/468 , C07K2317/24 , C07K2317/31 , C07K2317/33 , C07K2317/51 , C07K2317/515 , C07K2317/56 , C07K2317/565 , C07K2317/73 , C07K2317/92 , C07K2317/94 , G01N33/57492 , G01N2333/705
摘要: Mucin 16 (MUC16) is highly expressed in ovarian cancer and expression on cancer cells is shown to protect tumor cells from the immune system. The present invention provides novel full-length human IgG antibodies that bind to human and MUC16 (monospecific antibodies). The present invention also provides novel bispecific antibodies (bsAbs) that bind to both MUC16 and CD3 and activate T cells via the CD3 complex in the presence of MUC16-expressing tumors. According to certain embodiments, the present invention provides bispecific antigen-binding molecules comprising a first antigen-binding domain that specifically binds human and monkey CD3, and a second antigen-binding molecule that specifically binds human and monkey MUC16. In certain embodiments, the bispecific antigen-binding molecules of the present invention are capable of inhibiting the growth of tumors expressing MUC16. The bispecific antigen-binding molecules of the invention are useful for the treatment of diseases and disorders in which an upregulated or induced MUC16-targeted immune response is desired and/or therapeutically beneficial. For example, the bispecific antibodies of the invention are useful for the treatment of various cancers, including ovarian cancer. The present invention also includes anti-MUC16 antibody drug conjugates which inhibit tumor growth in vivo. In some embodiments, the anti-MUC16 antibodies are useful in diagnostic methods for identifying the presence of MUC16 in tissue and/or plasma samples.
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84.
公开(公告)号:US09657102B2
公开(公告)日:2017-05-23
申请号:US14031075
申请日:2013-09-19
CPC分类号: C07K16/2809 , A61K2039/505 , C07K16/2887 , C07K2317/21 , C07K2317/31 , C07K2317/33 , C07K2317/35 , C07K2317/734 , C07K2317/74 , C07K2317/92
摘要: The present invention provides antibodies that bind to CD3 and methods of using the same. According to certain embodiments, the antibodies of the invention bind human CD3 with high affinity and induce human T cell proliferation. The invention includes antibodies that bind CD3 and induce T cell-mediated killing of tumor cells. According to certain embodiments, the present invention provides bispecific antigen-binding molecules comprising a first antigen-binding domain that specifically binds human CD3, and a second antigen-binding molecule that specifically binds human CD20. In certain embodiments, the bispecific antigen-binding molecules of the present invention are capable of inhibiting the growth of B-cell tumors expressing CD20. The antibodies and bispecific antigen-binding molecules of the invention are useful for the treatment of diseases and disorders in which an upregulated or induced targeted immune response is desired and/or therapeutically beneficial. For example, the antibodies of the invention are useful for the treatment of various cancers as well as other CD20-related diseases and disorders.
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公开(公告)号:US20150266966A1
公开(公告)日:2015-09-24
申请号:US14661334
申请日:2015-03-18
IPC分类号: C07K16/28
摘要: The present invention provides bispecific antibodies that bind to CD3 and tumor antigens and methods of using the same. According to certain embodiments, the bispecific antibodies of the invention exhibit reduced effector functions and have a unique binding profile with regard to Fcγ receptors. The bispecific antibodies are engineered to efficiently induce T cell-mediated killing of tumor cells. According to certain embodiments, the present invention provides bispecific antigen-binding molecules comprising a first antigen-binding domain that specifically binds human CD3, a second antigen-binding molecule that specifically binds human CD20, and an Fc domain that binds Fcγ receptors with a specific binding pattern. In certain embodiments, the bispecific antigen-binding molecules of the present invention are capable of inhibiting the growth of B-cell or melanoma tumors expressing CD20. The bispecific antibodies of the invention are useful for the treatment of various cancers as well as other CD20-related diseases and disorders.
摘要翻译: 本发明提供了结合CD3和肿瘤抗原的双特异性抗体及其使用方法。 根据某些实施方案,本发明的双特异性抗体表现出降低的效应子功能并且具有关于Fcγ受体的独特结合特征。 双特异性抗体被工程化以有效诱导T细胞介导的杀伤肿瘤细胞。 根据某些实施方案,本发明提供双特异性抗原结合分子,其包含特异性结合人CD3的第一抗原结合结构域,特异性结合人CD20的第二抗原结合分子和与特异性结合Fcγ受体的Fc结构域 绑定模式。 在某些实施方案中,本发明的双特异性抗原结合分子能够抑制表达CD20的B细胞或黑素瘤肿瘤的生长。 本发明的双特异性抗体可用于治疗各种癌症以及其它与CD20相关的疾病和病症。
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公开(公告)号:US20150191534A1
公开(公告)日:2015-07-09
申请号:US14524164
申请日:2014-10-27
IPC分类号: C07K16/18
CPC分类号: C07K16/22 , A61K2039/505 , C07K16/18 , C07K2317/21 , C07K2317/30 , C07K2317/33 , C07K2317/34 , C07K2317/56 , C07K2317/565 , C07K2317/73 , C07K2317/732 , C07K2317/734 , C07K2317/76 , C07K2317/92
摘要: The present invention provides methods of treating, ameliorating, or inhibiting tumor growth, cancer, or pathological angiogenesis by administering to a subject in need thereof a human antibody or fragment thereof that specifically binds to human delta-like ligand 4 (hDll4) and blocks hDll4 binding to a Notch receptor. The anti-hDll4 antibody or fragment thereof of the present invention have a high affinity with the KD of 500 pM or less, as measured by surface plasmon resonance.
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公开(公告)号:US20240158529A1
公开(公告)日:2024-05-16
申请号:US18420588
申请日:2024-01-23
发明人: David DiLillo , Aynur Hermann , Jessica Kirshner , Kara Olson , Olga Sineshchekova , Eric Smith , Erica Ullman
IPC分类号: C07K16/28 , A61K39/395 , A61K45/06 , A61P35/00
CPC分类号: C07K16/2896 , A61K39/3955 , A61K45/06 , A61P35/00 , C07K16/2809 , C07K16/2818 , C07K16/2878 , C07K16/2887 , A61K2039/507
摘要: CD38 is expressed on malignant plasma cells. CD28 is a costimulatory molecule required for T-cell activation and survival. Provided herein are novel anti-CD38 antibodies, anti-CD28 antibodies, and bispecific antibodies (bsAbs) that bind to both CD38 and CD28 and act as costimulatory agents to activate T cells via binding CD80 and/or CD86. In certain embodiments, the bispecific antigen-binding molecules of the present invention are capable of inhibiting the growth of tumors expressing CD38. The bispecific antigen-binding molecules of the invention are useful for the treatment of diseases and disorders in which an upregulated or induced CD38-targeted immune response is desired and/or therapeutically beneficial. For example, the bispecific antibodies of the invention are useful for the treatment of various cancers, including multiple myeloma, lymphoma, and leukemia.
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公开(公告)号:US11952430B2
公开(公告)日:2024-04-09
申请号:US17967418
申请日:2022-10-17
发明人: Lauric Haber , Jennifer A. Finney , Ryan McKay , Eric Smith , Chia-Yang Lin
IPC分类号: C07K16/00 , C07K14/725 , C07K14/74 , C07K16/46
CPC分类号: C07K16/468 , C07K14/7051 , C07K14/70539 , C07K2317/31 , C07K2317/52 , C07K2317/55 , C07K2317/622
摘要: The present invention provides multispecific antigen-binding molecules that bind both a T-cell antigen (e.g., CD3) and a target antigen (e.g., a tumor associated antigen, a viral or bacterial antigen), and which include a single polypeptide chain that is multivalent (e.g., bivalent) with respect to T-cell antigen binding, and uses thereof.
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公开(公告)号:US20230279113A1
公开(公告)日:2023-09-07
申请号:US17890078
申请日:2022-08-17
发明人: Andrew J. Murphy , Dimitris Skokos , Janelle Waite , Erica Ullman , Aynur Hermann , Eric Smith , Lauric Haber , George D. Yancopoulos , Alison Crawford
IPC分类号: C07K16/28 , A61P35/00 , A61K39/395 , C07K16/30
CPC分类号: C07K16/2818 , A61K39/3955 , A61P35/00 , C07K16/2809 , C07K16/3092 , A61K2039/507
摘要: The present invention provides bispecific antigen-binding molecules comprising a first antigen-binding domain that specifically binds human CD28, and a second antigen-binding molecule that specifically binds human MUC16. In certain embodiments, the bispecific antigen-binding molecules of the present invention are capable of inhibiting the growth of tumors expressing MUC16, such as ovarian tumors. The antibodies and bispecific antigen-binding molecules of the invention are useful for the treatment of diseases and disorders in which an up-regulated or induced targeted immune response is desired and/or therapeutically beneficial.
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公开(公告)号:US11725034B2
公开(公告)日:2023-08-15
申请号:US17709706
申请日:2022-03-31
发明人: Jiaxi Wu , Tong Zhang , Maria del Pilar Molina-Portela , Eric Smith , Chia-Yang Lin , Thomas Craig Meagher
IPC分类号: C07K14/55 , A61K47/68 , A61P35/00 , C07K14/715 , A61K38/20 , A61K38/00 , A61K35/17 , C07K14/74 , C07K14/725 , C07K14/705
CPC分类号: C07K14/55 , A61K35/17 , A61K38/2013 , A61K47/6849 , A61P35/00 , C07K14/7051 , C07K14/70517 , C07K14/70539 , C07K14/7155 , A61K38/00 , C07K2319/30
摘要: The present disclosure relates to IL2 agonists with improved therapeutic profiles.
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