Blood Coagulation Factor VIII Activation-Enhancing Antibodies
    1.
    发明申请
    Blood Coagulation Factor VIII Activation-Enhancing Antibodies 有权
    血液凝固因子VIII激活增强抗体

    公开(公告)号:US20090297503A1

    公开(公告)日:2009-12-03

    申请号:US12395909

    申请日:2009-03-02

    IPC分类号: A61K39/395 C07K16/00 A61P7/00

    摘要: For the first time, the present invention provides antibodies that enhance the generation of activated blood coagulation factor VIII. The antibodies enhance the cleavage of blood coagulation factor VIII at the Arg of position 372 and suppress the cleavage at the Arg of position 336 by recognizing and binding to the A2 domain of blood coagulation Factor VIII. Such antibodies are expected to be useful in preventing or treating diseases that develop or progress due to decrease or loss of the blood coagulation factor VIII activity, for example, hemophilia A, acquired hemophilia, and von Willebrand's disease.

    摘要翻译: 本发明首次提供增强活化凝血因子VIII产生的抗体。 抗体增强了位置372的Arg处的凝血因子VIII的切割,并通过识别和结合凝血因子VIII的A2结构域来抑制位置336的Arg的切割。 预期这样的抗体可用于预防或治疗由于凝血因子VIII活性降低或丧失而发展或进展的疾病,例如血友病A,获得性血友病和血管性血友病。

    Blood coagulation factor VIII activation-enhancing antibodies
    2.
    发明授权
    Blood coagulation factor VIII activation-enhancing antibodies 有权
    血液凝固因子VIII激活增强抗体

    公开(公告)号:US08252287B2

    公开(公告)日:2012-08-28

    申请号:US12395909

    申请日:2009-03-02

    IPC分类号: A61K39/395

    摘要: For the first time, the present invention provides antibodies that enhance the generation of activated blood coagulation factor VIII. The antibodies enhance the cleavage of blood coagulation factor VIII at the Arg of position 372 and suppress the cleavage at the Arg of position 336 by recognizing and binding to the A2 domain of blood coagulation Factor VIII. Such antibodies are expected to be useful in preventing or treating diseases that develop or progress due to decrease or loss of the blood coagulation factor VIII activity, for example, hemophilia A, acquired hemophilia, and von Willebrand's disease.

    摘要翻译: 本发明首次提供增强活化凝血因子VIII产生的抗体。 抗体增强了位置372的Arg处的凝血因子VIII的切割,并通过识别和结合凝血因子VIII的A2结构域来抑制位置336的Arg的切割。 预期这样的抗体可用于预防或治疗由于凝血因子VIII活性降低或丧失而发展或进展的疾病,例如血友病A,获得性血友病和血管性血友病。