摘要:
Die vorliegende Anmeldung betrifft neuartige Binder-Prodrug-Konjugate (APDCs), bei denen Binder mit inaktiven Vorläuferverbindungen von Kinesin Spindel Protein-Inhibitoren konjugiert werden, sowie Antikörper-Wirkstoff-Konjugate ADCs und Verfahren zur Herstellung dieser APDCs bzw. ADCs.
摘要:
The aim of the present invention is to provide substances which show an apoptotic effect after administration in a relatively low concentration and can thus be useful for cancer therapy. To achieve this aim, the invention provides conjugates of an aglycosylated or aglycosyl anti-TWEAKR antibody with KSP inhibitors of formula (I), wherein one or more of the compounds of formula (I) is or are connected to the antibody via a linker L. Aglycosylated antibodies are antibodies which have no glycans at the preserved N-binding site in the CH2 domain of the Fc region. The antibody is preferably a human, humanised or chimeric monoclonal antibody. More preferably, the antibody is an anti-TWEAKR antibody, which specifically binds to the amino acid D in position 47 (D47) of TWEAKR (SEQ ID NO:169), in particular the anti-TWEAKR antibody TPP-2658.
摘要翻译:本发明的目的是提供以较低浓度给药后显示细胞凋亡效应的物质,因此可用于癌症治疗。 为了实现该目的,本发明提供了无糖基化或无糖基化抗TWEAKR抗体与式(I)的KSP抑制剂的缀合物,其中一种或多种式(I)化合物通过接头L与抗体连接 。糖基化抗体是在Fc区的CH2结构域的保存的N-结合位点不含聚糖的抗体。 该抗体优选是人类,人源化或嵌合单克隆抗体。 更优选地,抗体是抗TWEAKR抗体,其特异性结合TWEAKR(SEQ ID NO:169)的位置47(D47)中的氨基酸D,特别是抗TWEAKR抗体TPP-2658。
摘要:
The invention relates to site specific homogeneous binder drug conjugates of kinesin spindle protein inhibitors, to active metabolites of these conjugates, to processes for preparing these conjugates, to the use of these conjugates for the treatment and/or prophylaxis of diseases and to the use of these conjugates for preparing medicaments for treatment and/or prevention of diseases, in particular hyperproliferative and/or angiogenic disorders such as, for example, cancer diseases. Such treatments can be carried out as monotherapy or else in combination with other medicaments or further therapeutic measures.
摘要:
The invention relates to novel antibody prodrug conjugates (ADCs) in which antibodies with inactive precursor compounds of kinesin spindel protein-inhibitors are conjugated, and to antibody drug conjugate (ADCs) and to a method for producing said APDCs or ADCs.
摘要:
Die vorliegende Anmeldung betrifft neuartige Binder-Prodrug-Konjugate (APDCs), bei denen Binder mit inaktiven Vorläuferverbindungen von Kinesin Spindel Protein-Inhibitoren konjugiert werden, sowie Antikörper-Wirkstoff-Konjugate ADCs und Verfahren zur Herstellung dieser APDCs bzw. ADCs.
摘要:
The invention relates to novel antibody drug conjugates (ADCs), active metabolites of said ADCs, to methods for producing said ADCs, to the use of said ADCs for the treatment and/or prevention of diseases, and to the use of said ADCs for the production of medicaments for the treatment and/or prevention of diseases, in particular hyperproliferative and angiogenic diseases, such as cancer diseases. Such treatments can be effected as monotherapy or else in combination with other medicaments or further therapeutic measures.