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    • 107. 发明申请
    • NOVEL B7-H3 BINDING MOLECULES, ANTIBODY DRUG CONJUGATES THEREOF AND METHODS OF USE THEREOF
    • 新的B7-H3结合分子,抗体药物偶联物及其使用方法
    • WO2017180813A1
    • 2017-10-19
    • PCT/US2017/027317
    • 2017-04-13
    • MACROGENICS, INC.
    • LOO, Deryk, T.HUANG, LingJOHNSON, Leslie, S.SON, ThomasSCRIBNER, JuniperBONVINI, Ezio
    • A61K39/395A61K47/68C07K16/28
    • The present invention is directed to novel B7-H3-binding molecules capable of binding to human and non-human B7-H3, and in particular to such molecules that are cross-reactive with B7-H3 of a non-human primate (e.g., a cynomolgus monkey). The invention additionally pertains to B7-H3-binding molecules that comprise Variable Light Chain and/or Variable Heavy Chain (VH) Domains that have been humanized and/or deimmunized so as to exhibit a reduced immunogenicity upon administration to recipient subjects. The invention particularly pertains to bispecific, trispecific or multispecific B7-H3-binding molecules, including bispecific diabodies, BiTEs, bispecific antibodies, trivalent binding molecules, etc. that comprise: (i) such B7-H3-binding Variable Domains and (ii) a domain capable of binding to an epitope of a molecule present on the surface of an effector cell. The invention also particularly pertains to a molecule that comprises the human B7-H3 binding domain of a humanized anti-human B7-H3 antibody conjugated to at least one drug moiety (a "B7-H3-ADC").
    • 本发明涉及能够结合人和非人B7-H3的新型B7-H3结合分子,特别是涉及与B7-H3交叉反应的分子 非人灵长类动物(例如食蟹猴)。 本发明另外涉及包含可变轻链和/或可变重链(VH)结构域的B7-H3结合分子,所述可变轻链和/或可变重链(VH)结构域已被人源化和/或去免疫化,以便在给予受体对象时表现出降低的免疫原性。 本发明特别涉及双特异性,三特异性或多特异性B7-H3结合分子,包括双特异性双抗体,BiTE,双特异性抗体,三价结合分子等,其包含:(i)此类结合B7-H3的可变结构域和(ii) 能够结合存在于效应细胞表面上的分子的表位的结构域。 本发明还特别涉及包含与至少一个药物部分(“B7-H3-ADC”)缀合的人源化抗人B7-H3抗体的人B7-H3结合结构域的分子。