ANTIBODY COMPOSITION
    4.
    发明公开

    公开(公告)号:EP4130270A1

    公开(公告)日:2023-02-08

    申请号:EP21782017.4

    申请日:2021-04-01

    摘要: An object of the present invention is to provide an antibody composition, which exhibits an effector function more specifically for a target cell coexpressing two types of antigens that are different from each other and damages the target cell, and also can maintain affinity for the individual target antigens sufficiently high. The present invention relates to an antibody composition against a first antigen and a second antigen that are different from each other, including a first IgG half-molecule and a second IgG half-molecule, and relates to the first IgG half-molecule and the second IgG half-molecule constituting the antibody composition.

    BISPECIFIC ANTIBODY THAT BINDS TO CD3
    5.
    发明公开

    公开(公告)号:EP4105330A1

    公开(公告)日:2022-12-21

    申请号:EP21753218.3

    申请日:2021-02-12

    摘要: An object of the present invention is to provide a bispecific antibody that binds to CD3 or a bispecific antibody fragment thereof. The present invention relates to a bispecific antibody that binds to CD3 or a bispecific antibody fragment thereof, a DNA encoding the bispecific antibody or the bispecific antibody fragment thereof, a vector containing the DNA, a hybridoma and a transformant that produce the bispecific antibody or the bispecific antibody fragment thereof, a method for producing the bispecific antibody or the bispecific antibody fragment thereof, therapeutic and diagnostic agents containing the bispecific antibody or the bispecific antibody fragment thereof, therapeutic and diagnostic methods using the bispecific antibody or the bispecific antibody fragment thereof, and a reagent for detection or measurement containing the bispecific antibody or the bispecific antibody fragment thereof.

    DCR3 VARIANT
    6.
    发明公开
    DCR3 VARIANT 审中-公开

    公开(公告)号:EP4056232A1

    公开(公告)日:2022-09-14

    申请号:EP20864177.9

    申请日:2020-09-11

    摘要: An object of the present invention is to provide a DcR3 variant that has binding activity (preferably neutralizing activity) to a ligand of DcR3, and that results in a decreased amount of aggregates as compared to wild-type DcR3 when produced using a cell derived from a mammal as a host, and/or that exhibits improved in vivo kinetics; a DNA encoding the DcR3 variant; a vector including the DNA; a transformant obtained by introducing the vector; a method for producing a variant using the transformant; and a prophylactic or therapeutic agent for an autoimmune disease, an inflammatory disease or an allergic disease including the variant as an active ingredient, and, in order to achieve the object, the present invention provides a DcR3 variant including a part of DcR3 and a part of a TNF superfamily molecule.

    METHOD FOR PURIFYING ANTIBODY USING ADSORBENT

    公开(公告)号:EP4006047A1

    公开(公告)日:2022-06-01

    申请号:EP20846472.7

    申请日:2020-07-29

    IPC分类号: C07K1/14 C07K16/00 C12P21/08

    摘要: The purpose of the present invention is to provide: a method for purifying an antibody in non-adsorption mode using an inorganic compound that contains silicon dioxide and aluminum oxide, as a method for producing an antibody at a lower cost than the prior art; a method for producing an antibody that includes the purification method; and an antibody, etc., produced by the production method. The present invention pertains to a method for purifying an antibody in non-adsorption mode using an inorganic compound that contains silicon dioxide and aluminum oxide, a method for producing an antibody that includes the purification method, and an antibody produced by the production method.

    ALPHA, BETA-UNSATURATED AMIDE COMPOUND
    10.
    发明公开

    公开(公告)号:EP3712129A1

    公开(公告)日:2020-09-23

    申请号:EP18819602.6

    申请日:2018-06-22

    摘要: An object of the present invention is to provide an α,β-unsaturated amide compound or a pharmaceutically acceptable salt or the like thereof having anticancer activity and the like. The α,β-unsaturated amide compound represented by the following formula (I) or a pharmaceutically acceptable salt or the like thereof has anticancer activity and the like:

    [wherein, "A" represents optionally substituted heterocyclic diyl,
    R 1 represents hydrogen atom or optionally substituted lower alkyl,
    R 2 represents optionally substituted aryl, optionally substituted cycloalkyl, optionally substituted aliphatic heterocyclic group or optionally substituted aromatic heterocyclic group,
    X represents -O-, -S-, -SO 2 -, -NR X1 - (wherein, R X1 represents hydrogen atom or lower alkyl), -CHR X2 - (wherein, R X2 represents hydrogen atom or hydroxy), -CH=CH-, -CO- or -NH-CO-, and
    n1 and n2 are the same or different, and each represents 0 or 1].