Method for predicting the response to a treatment
    1.
    发明申请
    Method for predicting the response to a treatment 失效
    预测治疗反应的方法

    公开(公告)号:US20070037228A1

    公开(公告)日:2007-02-15

    申请号:US11438033

    申请日:2006-05-19

    IPC分类号: G01N33/574

    摘要: The invention is related to a method of predicting the response to a treatment with a HER inhibitor in a patient comprising the steps of assessing a biomarker or a combination of biomarkers selected from the group consisting of amphiregulin, an epidermal growth factor, a transforming growth factor alpha, and a HER2 biomarker in a biological sample from the patient and predicting the response to the treatment with the HER inhibitor in the patient by evaluating the results of the first step. Further uses and methods wherein these markers are used are disclosed.

    摘要翻译: 本发明涉及预测患者中用HER抑制剂治疗反应的方法,其包括以下步骤:评估生物标志物或生物标志物的组合,所述生物标志物或选自下组的生物标志物组合,所述生物标志物是由两性调节蛋白,表皮生长因子,转化生长因子 α和来自患者的生物样品中的HER2生物标志物,并通过评估第一步的结果预测患者中用HER抑制剂治疗的反应。 公开了其中使用这些标记的其它用途和方法。

    METHOD FOR PREDICTING THE RESPONSE TO A TREATMENT
    2.
    发明申请
    METHOD FOR PREDICTING THE RESPONSE TO A TREATMENT 审中-公开
    预防治疗反应的方法

    公开(公告)号:US20100112603A1

    公开(公告)日:2010-05-06

    申请号:US12624443

    申请日:2009-11-24

    IPC分类号: G01N33/53

    摘要: The invention is related to a method of predicting the response to a treatment with a HER inhibitor in a patient comprising the steps of assessing a biomarker or a combination of biomarkers selected from the group consisting of amphiregulin, an epidermal growth factor, a transforming growth factor alpha, and a HER2 biomarker in a biological sample from the patient and predicting the response to the treatment with the HER inhibitor in the patient by evaluating the results of the first step. Further uses and methods wherein these markers are used are disclosed.

    摘要翻译: 本发明涉及预测患者中用HER抑制剂治疗反应的方法,其包括以下步骤:评估生物标志物或生物标志物的组合,所述生物标志物或选自下组的生物标志物组合,所述生物标志物是由两性调节蛋白,表皮生长因子,转化生长因子 α和来自患者的生物样品中的HER2生物标志物,并通过评估第一步的结果预测患者中用HER抑制剂治疗的反应。 公开了其中使用这些标记的其它用途和方法。

    Method for predicting the response to a treatment
    3.
    发明授权
    Method for predicting the response to a treatment 失效
    预测治疗反应的方法

    公开(公告)号:US07700299B2

    公开(公告)日:2010-04-20

    申请号:US11438033

    申请日:2006-05-19

    摘要: The invention is related to a method of predicting the response to a treatment with a HER inhibitor in a patient comprising the steps of assessing a biomarker or a combination of biomarkers selected from the group consisting of amphiregulin, an epidermal growth factor, a transforming growth factor alpha, and a HER2 biomarker in a biological sample from the patient and predicting the response to the treatment with the HER inhibitor in the patient by evaluating the results of the first step. Further uses and methods wherein these markers are used are disclosed.

    摘要翻译: 本发明涉及预测患者中用HER抑制剂治疗反应的方法,其包括以下步骤:评估生物标志物或生物标志物的组合,所述生物标志物或选自下组的生物标志物组合,所述生物标志物是由两性调节蛋白,表皮生长因子,转化生长因子 α和来自患者的生物样品中的HER2生物标志物,并通过评估第一步的结果预测患者中用HER抑制剂治疗的反应。 公开了其中使用这些标记的其它用途和方法。

    MEANS AND METHODS FOR TREATING DLBCL
    4.
    发明申请
    MEANS AND METHODS FOR TREATING DLBCL 有权
    治疗DLBCL的方法和方法

    公开(公告)号:US20130287778A1

    公开(公告)日:2013-10-31

    申请号:US13881889

    申请日:2011-10-27

    IPC分类号: A61K39/395

    摘要: The present invention provides means and methods for treating diffuse large B cell lymphoma (DLBCL). Specifically, a bispecific CD19×CD3 antibody which engages T cells via its CD3 binding portion and concomitantly binds to CD19 on the surface of in particular, lymphoma cells via its CD19 binding portion (i.e. a bispecific T cell engager, “BiTE”) is administered for use in the treatment of tumorous mass of lymophoreticular tissue and/or extranodal lymphoma caused by DLBCL in a patient.

    摘要翻译: 本发明提供了治疗弥漫性大B细胞淋巴瘤(DLBCL)的方法和方法。 具体地,施用通过其CD3结合部分与T细胞接合并通过其CD19结合部分特别是淋巴瘤细胞表面(即双特异性T细胞募集体“BiTE”)并与CD19结合的双特异性CD19×CD3抗体) 用于治疗由DLBCL引起的淋巴管组织和/或结外淋巴瘤的肿瘤组织。

    TREATMENT OF PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA
    6.
    发明申请
    TREATMENT OF PEDIATRIC ACUTE LYMPHOBLASTIC LEUKEMIA 审中-公开
    治疗急性淋巴细胞白血病

    公开(公告)号:US20110262440A1

    公开(公告)日:2011-10-27

    申请号:US13127538

    申请日:2009-11-06

    申请人: Gerhard Zugmaier

    发明人: Gerhard Zugmaier

    摘要: The present invention relates to a method for the treatment, amelioration or elimination of pediatric acute lymphoblastic leukemia (ALL), the method comprising the administration of a pharmaceutical composition comprising a CD19×CD3 bispecific single chain antibody construct to a pediatric ALL patient in the need thereof.

    摘要翻译: 本发明涉及一种治疗,改善或消除儿科急性淋巴细胞白血病(ALL)的方法,所述方法包括向需要的儿科ALL患者施用包含CD19×CD3双特异性单链抗体构建体的药物组合物 其中。

    Means and methods for treating DLBCL
    8.
    发明授权
    Means and methods for treating DLBCL 有权
    治疗DLBCL的方法和方法

    公开(公告)号:US09192665B2

    公开(公告)日:2015-11-24

    申请号:US13881889

    申请日:2011-10-27

    摘要: The present invention provides means and methods for treating diffuse large B cell lymphoma (DLBCL). Specifically, a bispecific CD19×CD3 antibody which engages T cells via its CD3 binding portion and concomitantly binds to CD19 on the surface of in particular, lymphoma cells via its CD19 binding portion (i.e. a bispecific T cell engager, “BiTE”) is administered for use in the treatment of tumorous mass of lymophoreticular tissue and/or extranodal lymphoma caused by DLBCL in a patient.

    摘要翻译: 本发明提供了治疗弥漫性大B细胞淋巴瘤(DLBCL)的方法和方法。 具体地,施用通过其CD3结合部分与T细胞接合并通过其CD19结合部分特别是淋巴瘤细胞表面(即,双特异性T细胞募集体“BiTE”)同时结合CD19的双特异性CD19×CD3抗体) 用于治疗由DLBCL引起的淋巴管组织和/或结外淋巴瘤的肿瘤组织。

    TREATMENT OF ACUTE LYMPHOBLASTIC LEUKEMIA
    10.
    发明申请
    TREATMENT OF ACUTE LYMPHOBLASTIC LEUKEMIA 审中-公开
    急性淋巴细胞白血病治疗

    公开(公告)号:US20130323247A1

    公开(公告)日:2013-12-05

    申请号:US13127541

    申请日:2009-11-06

    摘要: The present invention relates to a method for the treatment, amelioration or elimination of acute lymphoblastic leukemia (ALL), the method comprising the administration of a pharmaceutical composition comprising a CD19xCD3 bispecific single chain antibody construct to an adult patient in the need thereof.

    摘要翻译: 本发明涉及一种治疗,改善或消除急性淋巴细胞白血病(ALL)的方法,所述方法包括向需要的成年患者施用包含CD19xCD3双特异性单链抗体构建体的药物组合物。