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公开(公告)号:EP3690050A1
公开(公告)日:2020-08-05
申请号:EP18860741.0
申请日:2018-09-27
发明人: TERANISHI, Yuri , KATO, Kazuki , KOGA, Hikaru , IGAWA, Tomoyuki , YAMAGUCHI, Kazuki , SOEDA, Tetsuhiro
IPC分类号: C12N15/13 , A61K39/395 , A61P7/04 , C07K16/36 , C07K16/46 , C12N1/15 , C12N1/19 , C12N1/21 , C12N5/10 , C12P21/08
摘要: Bispecific antibodies whose FIX activation-inhibiting activity is not elevated and whose FVIII cofactor function-substituting activity is elevated have been successfully discovered.
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公开(公告)号:EP3827024A1
公开(公告)日:2021-06-02
申请号:EP19840512.8
申请日:2019-07-22
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公开(公告)号:EP3812399A1
公开(公告)日:2021-04-28
申请号:EP19822018.8
申请日:2019-06-20
发明人: SAKASHITA, Takuya , SAVORY, Nasa , KATO, Kazuki , NARUSHIMA, Yuta , MURAKAMI, Ryuichi , IGAWA, Tomoyuki
IPC分类号: C07K16/46 , A61K39/395 , A61P35/00 , C07K16/28 , C07K16/30
摘要: In one embodiment, a multispecific antigen-binding molecule that recognizes an antigen on an antigen-presenting cell and an antigen on a target cell, which is capable of crosslinking the antigen-presenting cell and the target cell, is provided.
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公开(公告)号:EP3805400A1
公开(公告)日:2021-04-14
申请号:EP19814965.0
申请日:2019-06-03
摘要: In a non-limiting embodiment, the present invention relates to antigen-binding molecules containing an altered TRIM21-binding domain and having an altered cytosolic half-life; pharmaceutical compositions containing such an antigen-binding molecule; methods for using such an antigen-binding molecule; methods for increasing or decreasing the cytosolic half-life of an antigen-binding molecule containing a TRIM21-binding domain; and methods for producing an antigen-binding molecule containing an altered TRIM21-binding domain and having an increased or decreased cytosolic half-life. The present invention also relates to substitutions at specific positions in a TRIM21-binding domain that increase or decrease the cytosolic half-life of an antigen-binding molecule containing a TRIM21-binding domain.
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公开(公告)号:EP3492496A1
公开(公告)日:2019-06-05
申请号:EP17834452.9
申请日:2017-07-27
发明人: IGAWA, Tomoyuki , TERANISHI, Yuri , KATO, Kazuki , KOGA, Hikaru
摘要: The present invention provides light chain amino acid substitutions that improve the FVIII cofactor function-substituting activity of ACE910 (Emicizumab), novel light chains showing FVIII cofactor function-substituting activity, and heavy chain amino acid substitutions that improve the FVIII cofactor function-substituting activity of novel light chain-containing bispecific antibodies.
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