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    • 14. 发明申请
    • COMBINATION THERAPY
    • 联合治疗
    • WO2017214092A1
    • 2017-12-14
    • PCT/US2017/036075
    • 2017-06-06
    • MACROGENICS, INC.
    • BONVINI, EzioKOENIG, ScottJOHNSON, Leslie, S.MOORE, Paul, A.ALDERSON, Ralph, F.
    • A61K39/395C07K16/28A61P35/00A61P31/00
    • The present invention is directed to a combination therapy for the treatment of cancer and pathogen-associated diseases, that comprises the administration of: (I) a molecule (e.g., a diabody, an scFv, an antibody, a TandAb, etc.) capable of binding PD-I or a natural ligand of PD-I, and (2) a molecule (e.g., a diabody, a BiTe, a bispecific antibody, a CAR, etc.) capable of mediating the redirected killing of a target cell (e.g., a cancer cell or a pathogeninfected cell, etc.) expressing a Disease Antigen. The invention particularly concerns the embodiment in which the molecule capable of mediating the redirected killing of the target cell is a bispecific binding molecule that comprises a first epitope-binding site capable of immunospecifically binding an epitope of a cell surface molecule of an effector cell and a second epitope-binding site that is capable of immunospecifically binding an epitope of such target cells.
    • 本发明涉及用于治疗癌症和病原体相关疾病的组合疗法,其包括施用以下物质:(I)分子(例如双抗体,scFv,抗体 ,TandAb等),和(2)能够介导PD-1或PD-1的天然配体的分子(例如双抗体,BiTe,双特异性抗体,CAR等) 表达疾病抗原的靶细胞(例如,癌细胞或病原体感染的细胞等)的重定向杀死。 本发明特别涉及其中能够介导重定向杀死靶细胞的分子的双特异性结合分子的实施方案,其包含能够免疫特异性结合效应细胞的细胞表面分子的表位的第一表位结合位点和 第二表位结合位点,其能够免疫特异性地结合此类靶细胞的表位。
    • 15. 发明申请
    • PD-1-BINDING MOLECULES AND METHODS USE THEREOF
    • PD-1结合分子及其使用方法
    • WO2017019846A1
    • 2017-02-02
    • PCT/US2016/044430
    • 2016-07-28
    • MACROGENICS, INC.
    • SHAH, KalpanaSMITH, Douglas, H.LA MOTTE-MOHS, RossJOHNSON, Leslie, S.MOORE, Paul, A.BONVINI, EzioKOENIG, Scott
    • A61K39/00A61K39/395C07K16/00
    • A61K39/00A61K39/395C07K16/2803C07K16/2818C07K2317/24C07K2317/31C07K2317/33C07K2317/76
    • The present invention is directed to selected anti-PD-1 antibodies capable of binding to both cynomolgus monkey PD-1 and to human PD-1 : PD-1 mAb 1, PD-1 mAb 2, PD-1 mAb 3, PD-1 mAb 4, PD-1 mAb 5, PD-1 mAb 6, PD-1 mAb 7, PD-1 mAb 8, PD-1 mAb 9, PD-1 mAb 10, PD-1 mAb 11, PD-1 mAb 12, PD-1 mAb 13, PD-1 mAb 14, or PD-1 mAb 15, and to humanized and chimeric versions of such antibodies. The invention additionally pertains to PD-1 -binding molecules that comprise PD-1 binding fragments of such anti-PD-1 antibodies, immunocongugates, and to bispecific molecules, including diabodies, BiTEs, bispecific antibodies, etc., that comprise (i) such PD-1 -binding fragments, and (ii) a domain capable of binding an epitope of a molecule involved in regulating an immune check point present on the surface of an immune cells. The present invention also pertains to methods of using molecules that bind PD-1 for stimulating immune responses, as well as methods of detecting PD-1.
    • 本发明涉及能够结合食蟹猴PD-1和人PD-1的选择的抗PD-1抗体:PD-1mAb 1,PD-1mAb 2,PD-1mAb 3,PD- 1mAb 4,PD-1mAb 5,PD-1mAb 6,PD-1mAb 7,PD-1mAb 8,PD-1mAb 9,PD-1mAb 10,PD-1mAb 11,PD-1mAb 12,PD-1mAb 13,PD-1mAb 14或PD-1mAb 15,以及这些抗体的人源化和嵌合形式。 本发明还涉及包含PD-1结合片段的PD-1结合分子,所述PD-1结合片段包含抗PD-1抗体,免疫接种物以及双特异性分子,包括双抗体,BiTE,双特异性抗体等,其包含(i) 这样的PD-1结合片段,和(ii)能够结合涉及调节免疫细胞表面上存在的免疫检测点的分子表位的结构域。 本发明还涉及使用结合PD-1的分子刺激免疫应答的方法,以及检测PD-1的方法。