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公开(公告)号:US20090030183A1
公开(公告)日:2009-01-29
申请号:US12206275
申请日:2008-09-08
申请人: Poul Baad Rasmussen , Joern Drustrup , Grethe Rasmussen , Anders Hjelholt Pedersen , Hans Thalsgard Schambye , Kim Vilbour Andersen , Claus Bornaes
发明人: Poul Baad Rasmussen , Joern Drustrup , Grethe Rasmussen , Anders Hjelholt Pedersen , Hans Thalsgard Schambye , Kim Vilbour Andersen , Claus Bornaes
IPC分类号: C07K14/565 , C12P21/02 , C12N15/19 , C12N5/10 , C12N15/85
CPC分类号: A61K9/0019 , A61K9/0073 , A61K31/724 , A61K38/21 , A61K38/215 , A61K47/40 , A61K47/60 , A61K47/6951 , B82Y5/00 , C07K14/565 , A61K2300/00
摘要: The invention relates to a conjugate exhibiting interferon β (IFNB) activity and comprising at least one first non-polypeptide moiety covalently attached to an IFNB polypeptide, the amino acid sequence of which differs from that of wildtype human IFNB in at least one introduced and at least one removed amino acid residue comprising an attachment group for said first non-polypeptide moiety. The first non-polypeptide moiety is e.g. a polymer molecule or a sugar moiety. The conjugate finds particular use in therapy. The invention also relates to a glycosylated variant of a parent IFNB polypeptide comprising at least one in vivo glycosylation site, wherein an amino acid residue of said parent polypeptide located close to said glycosylation site has been modified to obtain the variant polypeptide having an increased glycosylation as compared to the glycosylation of the parent polypeptide.
摘要翻译: 本发明涉及一种表现出干扰素β(IFNB)活性的缀合物,其包含共价连接到IFNB多肽的至少一个第一非多肽部分,所述第一非多肽部分与至少一个引入的和在 至少一个除去的氨基酸残基,其包含所述第一非多肽部分的连接基团。 第一非多肽部分是例如。 聚合物分子或糖部分。 该缀合物在治疗中特别有用。 本发明还涉及包含至少一个体内糖基化位点的母体IFNB多肽的糖基化变体,其中位于所述糖基化位点附近的所述亲本多肽的氨基酸残基已被修饰以获得具有增加的糖基化的变体多肽作为 与母体多肽的糖基化相比。
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公开(公告)号:US07338788B2
公开(公告)日:2008-03-04
申请号:US10351189
申请日:2003-01-24
CPC分类号: B82Y5/00 , A61K38/215
摘要: The present invention provides new interferon β conjugates, methods of preparing such conjugates and the use of such conjugates in therapy, in particular for the treatment of multiple sclerosis.
摘要翻译: 本发明提供新的干扰素β缀合物,制备这种缀合物的方法以及这种缀合物在治疗中的用途,特别是用于治疗多发性硬化。
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公开(公告)号:US07238344B2
公开(公告)日:2007-07-03
申请号:US10325720
申请日:2002-12-19
CPC分类号: B82Y5/00 , A61K38/215
摘要: The present invention provides new interferon β conjugates, methods of preparing such conjugates and the use of such conjugates in therapy, in particular for the treatment of multiple sclerosis.
摘要翻译: 本发明提供新的干扰素β缀合物,制备这种缀合物的方法以及这种缀合物在治疗中的用途,特别是用于治疗多发性硬化。
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公开(公告)号:US07144574B2
公开(公告)日:2006-12-05
申请号:US10084706
申请日:2002-02-26
CPC分类号: B82Y5/00 , A61K9/0019 , A61K31/724 , A61K38/21 , A61K38/215 , A61K47/40 , A61K47/6951 , C07K14/565 , A61K2300/00
摘要: The invention relates to a conjugate exhibiting interferon β (IFNB) activity and comprising at least one first non-polypeptide moiety covalently attached to an IFNB polypeptide, the amino acid sequence of which differs from that of wildtype human IFNB in at least one introduced and at least one removed amino acid residue comprising an attachment group for said first non-polypeptide moiety. The first non-polypeptide moiety is e.g. a polymer molecule or a sugar moiety. The conjugate finds particular use in therapy. The invention also relates to a glycosylated variant of a parent IFNB polypeptide comprising at least one in vivo glycosylation site, wherein an amino acid residue of said parent polypeptide located close to said glycosylation site has been modified to obtain the variant polypeptide having an increased glycosylation as compared to the glycosylation of the parent polypeptide.
摘要翻译: 本发明涉及一种表现出干扰素β(IFNB)活性的缀合物,其包含共价连接到IFNB多肽的至少一个第一非多肽部分,所述第一非多肽部分与至少一个引入的和在 至少一个除去的氨基酸残基,其包含所述第一非多肽部分的连接基团。 第一非多肽部分是例如。 聚合物分子或糖部分。 该缀合物在治疗中特别有用。 本发明还涉及包含至少一个体内糖基化位点的母体IFNB多肽的糖基化变体,其中位于所述糖基化位点附近的所述亲本多肽的氨基酸残基已被修饰以获得具有增加的糖基化的变体多肽作为 与母体多肽的糖基化相比。
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公开(公告)号:US07431921B2
公开(公告)日:2008-10-07
申请号:US10609296
申请日:2003-06-27
CPC分类号: A61K9/0019 , A61K9/0073 , A61K31/724 , A61K38/21 , A61K38/215 , A61K47/40 , A61K47/60 , A61K47/6951 , B82Y5/00 , C07K14/565 , A61K2300/00
摘要: The invention relates to a conjugate exhibiting interferon β (IFNB) activity and comprising at least one first non-polypeptide moiety covalently attached to an IFNB polypeptide, the amino acid sequence of which differs from that of wildtype human IFNB in at least one introduced and at least one removed amino acid residue comprising an attachment group for said first non-polypeptide moiety. The first non-polypeptide moiety is e.g. a polymer molecule or a sugar moiety. The conjugate finds particular use in therapy. The invention also relates to a glycosylated variant of a parent IFNB polypeptide comprising at least one in vivo glycosylation site, wherein an amino acid residue of said parent polypeptide located close to said glycosylation site has been modified to obtain the variant polypeptide having an increased glycosylation as compared to the glycosylation of the parent polypeptide.
摘要翻译: 本发明涉及一种表现出干扰素β(IFNB)活性的缀合物,其包含共价连接到IFNB多肽的至少一个第一非多肽部分,所述第一非多肽部分与至少一个引入的和在 至少一个除去的氨基酸残基,其包含所述第一非多肽部分的连接基团。 第一非多肽部分是例如。 聚合物分子或糖部分。 该缀合物在治疗中特别有用。 本发明还涉及包含至少一个体内糖基化位点的母体IFNB多肽的糖基化变体,其中位于所述糖基化位点附近的所述亲本多肽的氨基酸残基已被修饰以获得具有增加的糖基化的变体多肽作为 与母体多肽的糖基化相比。
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公开(公告)号:US07511024B2
公开(公告)日:2009-03-31
申请号:US11279541
申请日:2006-04-12
IPC分类号: C07H21/04
CPC分类号: C07K14/745 , A61K38/00 , A61K47/60 , A61K47/62 , C12N9/6437 , C12Y304/21021 , Y10S514/802
摘要: Conjugates of Factor VII (FVII) and Factor VIIa (FVIIA) are provided, as are methods for preparing them. Methods for producing novel polypeptides contributing to the production of such conjugates are provided. Methods of treatment by administering a FVII or FVIIa conjugate are provided.
摘要翻译: 提供因子VII(FVII)和因子VIIa(FVIIA)的缀合物,以及制备它们的方法。 提供了有助于制备这种缀合物的新型多肽的制备方法。 提供了通过施用FVII或FVIIa缀合物治疗的方法。
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公开(公告)号:US07442524B2
公开(公告)日:2008-10-28
申请号:US11423662
申请日:2006-06-12
IPC分类号: C07K14/745
CPC分类号: C07K14/745 , A61K38/00 , A61K47/60 , A61K47/62 , C12N9/6437 , C12Y304/21021 , Y10S514/802
摘要: Conjugates of Factor VII (FVII) and Factor VIIa (FVIIA) are provided, as are methods for preparing them. Methods for producing novel polypeptides contributing to the production of such conjugates are provided. Methods of treatment by administering a FVII or FVIIa conjugate are provided.
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公开(公告)号:US07414022B2
公开(公告)日:2008-08-19
申请号:US11426401
申请日:2006-06-26
IPC分类号: A61K38/00
CPC分类号: C07K14/745 , A61K38/00 , A61K47/60 , A61K47/62 , C12N9/6437 , C12Y304/21021 , Y10S514/802
摘要: Conjugates of Factor VII (FVII) and Factor VIIa (FVIIA) are provided, as are methods for preparing them. Methods for producing novel polypeptides contributing to the production of such conjugates are provided. Methods of treatment by administering a FVII or FVIIa conjugate are provided.
摘要翻译: 提供因子VII(FVII)和因子VIIa(FVIIA)的缀合物,以及制备它们的方法。 提供了有助于制备这种缀合物的新型多肽的制备方法。 提供了通过施用FVII或FVIIa缀合物治疗的方法。
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公开(公告)号:US08084591B2
公开(公告)日:2011-12-27
申请号:US11423622
申请日:2006-06-12
IPC分类号: C07H21/04 , C07K14/755 , C12P21/00 , A61K38/36
CPC分类号: C07K14/745 , A61K38/00 , A61K47/60 , A61K47/62 , C12N9/6437 , C12Y304/21021 , Y10S514/802
摘要: Conjugates of Factor VII (FVII) and Factor VIIa (FVIIA) are provided, as are methods for preparing them. Methods for producing novel polypeptides contributing to the production of such conjugates are provided. Methods of treatment by administering a FVII or FVIIa conjugate are provided.
摘要翻译: 提供因子VII(FVII)和因子VIIa(FVIIA)的缀合物,以及制备它们的方法。 提供了有助于制备这种缀合物的新型多肽的制备方法。 提供了通过施用FVII或FVIIa缀合物治疗的方法。
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公开(公告)号:US07517974B2
公开(公告)日:2009-04-14
申请号:US11396314
申请日:2006-03-30
IPC分类号: C07H21/04 , C12P21/00 , A61K38/00 , A61K38/16 , C07K14/745
CPC分类号: C07K14/745 , A61K38/00 , A61K47/60 , A61K47/62 , C12N9/6437 , C12Y304/21021 , Y10S514/802
摘要: Conjugates of Factor VII (FVII) and Factor VIIa (FVIIA) are provided, as are methods for preparing them. Methods for producing novel polypeptides contributing to the production of such conjugates are provided. Methods of treatment by administering a FVII or FVIIa conjugate are provided.
摘要翻译: 提供因子VII(FVII)和因子VIIa(FVIIA)的缀合物,以及制备它们的方法。 提供了有助于制备这种缀合物的新型多肽的制备方法。 提供了通过施用FVII或FVIIa缀合物治疗的方法。
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