COMBINATION THERAPY OF A TYPE II ANTI-CD20 ANTIBODY WITH A PROTEASOME INHIBITOR
    9.
    发明申请
    COMBINATION THERAPY OF A TYPE II ANTI-CD20 ANTIBODY WITH A PROTEASOME INHIBITOR 审中-公开
    抗抑郁剂类型II抗CD20抗体的联合治疗

    公开(公告)号:US20110200598A1

    公开(公告)日:2011-08-18

    申请号:US13075946

    申请日:2011-03-30

    IPC分类号: A61K39/395 A61P35/00

    摘要: The present invention is directed to a combination therapy involving a type II anti-CD20 antibody and a proteasome inhibitor for the treatment of a patient suffering from cancer, particularly a CD20-expressing cancer. An aspect of the invention is a composition comprising a type II anti-CD20 antibody and a proteasome inhibitor. Another aspect of the invention is a kit comprising a type II anti-CD20 antibody and a proteasome inhibitor. Yet another aspect of the invention is a method for the treatment of a patient suffering from cancer comprising co-administering, to a patient in need of such treatment, a type II anti-CD20 antibody and a proteasome inhibitor.

    摘要翻译: 本发明涉及涉及用于治疗患有癌症的患者,特别是表达CD20的癌症的II型抗-CD20抗体和蛋白酶体抑制剂的组合疗法。 本发明的一个方面是包含II型抗CD20抗体和蛋白酶体抑制剂的组合物。 本发明的另一方面是包含II型抗CD20抗体和蛋白酶体抑制剂的试剂盒。 本发明的另一方面是治疗患有癌症的患者的方法,包括向需要这种治疗的患者共同施用II型抗CD20抗体和蛋白酶体抑制剂。

    Determination of apoptotic products in tumor patients undergoing therapy
    10.
    发明授权
    Determination of apoptotic products in tumor patients undergoing therapy 有权
    肿瘤患者接受治疗的凋亡产物的测定

    公开(公告)号:US07759071B2

    公开(公告)日:2010-07-20

    申请号:US11738899

    申请日:2007-04-23

    摘要: The present invention concerns a method for the determination of apoptotic products in samples taken from patients in which apoptosis is induced as a result of disease or therapy, which is characterized in that the concentration of the apoptotic products in samples taken from patients is correlated with the effectiveness of the therapy and thus serves as a follow-up for the therapy. The present invention in particular concerns a method in which the concentration of nucleosomes is determined in serum samples of tumour patients in order to assess the effectiveness of tumour therapy. Furthermore the present invention also concerns the use of a method according to the invention to determine the effectiveness of therapy in tumour patients who are subjected to a radiotherapy or chemotherapy treatment as well as in patients after an acute ischaemic event or after hypothermia treatment.

    摘要翻译: 本发明涉及一种用于测定来自患者的凋亡产物的方法,其中所述样品取自患有由疾病或治疗引起的细胞凋亡的患者,其特征在于,取自患者的样品中的凋亡产物的浓度与 治疗的有效性,从而作为治疗的后续行动。 本发明特别涉及一种方法,其中在肿瘤患者的血清样品中测定核小体的浓度,以评估肿瘤治疗的有效性。 此外,本发明还涉及根据本发明的方法用于确定经受放射治疗或化疗治疗的肿瘤患者以及急性缺血事件或低体温治疗后患者的治疗效果的用途。