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公开(公告)号:US11230603B2
公开(公告)日:2022-01-25
申请号:US16791937
申请日:2020-02-14
发明人: Sophie Lucas , Pierre Coulie , Julia Cuende Villasur , Laure Dumoutier , Jean-Christophe Renauld , Sebastian van der Woning , Michael Saunders , Hans De Haard , Gitte De Boeck
摘要: The present invention relates to a protein binding to GARP in the presence of TGF-β and uses thereof.
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公开(公告)号:US20200024344A1
公开(公告)日:2020-01-23
申请号:US16435166
申请日:2019-06-07
申请人: argenx BVBA
发明人: Hans de Haard , Peter Ulrichts , Thierry Cousin , Nicolas Leupin , Torsten Dreier , Tonke Van Bragt
摘要: A method is disclosed for the treatment of human subjects diagnosed with immune thrombocytopenia (ITP). The method comprises administering to a human subject a human neonatal Fc receptor (hFcRn) antagonist, optionally in combination with standard-of-care ITP treatment. In certain embodiments, the hFcRn antagonist is efgartigimod (ARGX-113). Standard-of-care ITP treatment may comprise administration of corticosteroids, immunosuppressants, and/or thrombopoietin receptor (TPO-R) agonists.
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公开(公告)号:US20180215833A1
公开(公告)日:2018-08-02
申请号:US15854312
申请日:2017-12-26
申请人: argenx BVBA
发明人: Anna HULTBERG , Michael SAUNDERS , Johannes DE HAARD , Els FESTJENS , Natalie DE JONGE , Paolo MICHIELI , Cristina Basilico , Torsten DREIER
摘要: The present invention relates to antibodies that specifically bind to the human c-Met receptor protein and that act as strict antagonists of hepatocyte growth factor (HGF)-mediated activation of the c-Met receptor and also inhibit HGF-independent activation of the human c-Met protein.
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公开(公告)号:US20220119509A1
公开(公告)日:2022-04-21
申请号:US17491656
申请日:2021-10-01
申请人: argenx BVBA
IPC分类号: C07K16/18
摘要: Provided are antibodies and antigen-binding fragments thereof that bind specifically to human complement factor C2 and are capable of inhibiting activation of the classical and lectin pathways of the complement system. The antibodies and antigen-binding fragment exhibit improved manufacturability, pharmacokinetics, and antigen sweeping. Also provided are pharmaceutical compositions comprising the antibodies and antigen-binding fragments, nucleic acids and vectors encoding the antibodies and antigen-binding fragments, host cells comprising the nucleic acids or vectors, and methods of making and using the antibodies and antigen-binding fragments. The antibodies and antigen-binding fragments can be used to inhibit the classical pathway of complement activation in a subject, e.g., a human. The antibodies and antigen-binding fragments can also be used to inhibit the lectin pathway of complement activation in a subject, e.g., a human.
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公开(公告)号:US20210324061A1
公开(公告)日:2021-10-21
申请号:US17096931
申请日:2020-11-12
发明人: Sebastian van der Woning , Filip Borgions , Torsten Dreier , Lore Mariën , Gitte De Boeck , Stéphanie Liénart , Sophie Lucas , Pierre Coulie
摘要: The present invention relates to antibodies and antigen binding fragments thereof, which bind to a complex of GARP and TGF-β1, particularly a complex of human GARP and human TGF-β1. These antibodies and antigen binding fragments exhibit a combination of advantageous properties including high affinity antigen binding and the ability to inhibit the release of active TGF-β from regulatory T cells. The antibodies and antigen binding fragments of the present invention are relatively resistant to deamidation, isomerization and oxidation, such that they display improved stability.
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公开(公告)号:US20200239554A1
公开(公告)日:2020-07-30
申请号:US16714264
申请日:2019-12-13
申请人: argenx BVBA
IPC分类号: C07K16/18
摘要: Provided are antibodies and antigen-binding fragments thereof that bind specifically to human complement factor C2 and are capable of inhibiting activation of the classical and lectin pathways of the complement system. The antibodies and antigen-binding fragment exhibit improved manufacturability, pharmacokinetics, and antigen sweeping. Also provided are pharmaceutical compositions comprising the antibodies and antigen-binding fragments, nucleic acids and vectors encoding the antibodies and antigen-binding fragments, host cells comprising the nucleic acids or vectors, and methods of making and using the antibodies and antigen-binding fragments. The antibodies and antigen-binding fragments can be used to inhibit the classical pathway of complement activation in a subject, e.g., a human. The antibodies and antigen-binding fragments can also be used to inhibit the lectin pathway of complement activation in a subject, e.g., a human.
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公开(公告)号:US20200157248A1
公开(公告)日:2020-05-21
申请号:US16599883
申请日:2019-10-11
申请人: argenx BVBA
摘要: The present invention relates to multispecific antibodies, for example bispecific antibodies, and methods for the isolation or purification of the same. The antibodies of the invention comprise first and second heavy chain-light chain pairings wherein each pairing comprises a distinct selective recognition site including one or more amino acid residues contributed from the heavy chain and the light chain of the pairing. The first and second selective recognition sites differ by at least one amino acid residue and can be differentially bound by first and second selective recognition agents according to the methods of the invention. Such methods facilitate the production of antibody preparations enriched for multispecific antibodies having the correct functional heavy chain-light chain pairings.
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公开(公告)号:US20180327487A1
公开(公告)日:2018-11-15
申请号:US15977449
申请日:2018-05-11
申请人: argenx BVBA
发明人: Sebastian Van der Woning , Filip Borgions , Torsten Dreier , Lore Mariën , Federica Linty , Gitte De Boeck , Hans De Haard , Stéphanie Liénart , Sophie Lucas , Pierre Coulie , Michael Saunders
CPC分类号: C07K16/22 , A61K2039/505 , C07K16/28 , C07K2317/22 , C07K2317/32 , C07K2317/33 , C07K2317/526 , C07K2317/55 , C07K2317/56 , C07K2317/565 , C07K2317/732 , C07K2317/76 , C07K2317/92 , C07K2317/94
摘要: The present invention relates to antibodies and antigen binding fragments thereof, which bind to a complex of GARP and TGF-β1, particularly a complex of human GARP and human TGF-β1. These antibodies and antigen binding fragments exhibit a combination of advantageous properties including high affinity antigen binding and the ability to inhibit the release of active TGF-β from regulatory T cells. The antibodies and antigen binding fragments of the present invention are relatively resistant to deamidation, isomerization and oxidation, such that they display improved stability.
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公开(公告)号:US20220177555A1
公开(公告)日:2022-06-09
申请号:US16606656
申请日:2018-05-10
申请人: argenx BVBA
IPC分类号: C07K16/18
摘要: Methods for preparing engineered antibodies exhibiting improved pH-dependent antigen binding are disclosed. The methods are based on introduction of histidine residues at a subset of defined amino acid positions within the antibody CDRs. The set of amino acid positions selected for histidine substitution is derived from a heat-map of histidine occurrence within the CDRs of functional antibodies from a natural antibody repertoire. The methods provide a simpler and less time-consuming approach to the identification of pH-dependent antibody variants.
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公开(公告)号:US11161900B2
公开(公告)日:2021-11-02
申请号:US16714264
申请日:2019-12-13
申请人: argenx BVBA
IPC分类号: C07K16/18 , A61K39/395 , A61K39/00
摘要: Provided are antibodies and antigen-binding fragments thereof that bind specifically to human complement factor C2 and are capable of inhibiting activation of the classical and lectin pathways of the complement system. The antibodies and antigen-binding fragment exhibit improved manufacturability, pharmacokinetics, and antigen sweeping. Also provided are pharmaceutical compositions comprising the antibodies and antigen-binding fragments, nucleic acids and vectors encoding the antibodies and antigen-binding fragments, host cells comprising the nucleic acids or vectors, and methods of making and using the antibodies and antigen-binding fragments. The antibodies and antigen-binding fragments can be used to inhibit the classical pathway of complement activation in a subject, e.g., a human. The antibodies and antigen-binding fragments can also be used to inhibit the lectin pathway of complement activation in a subject, e.g., a human.
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