Anti-human IL-21 monoclonal antibodies
    1.
    发明公开
    Anti-human IL-21 monoclonal antibodies 有权
    Monoklonale抗人IL-21-Antikörper

    公开(公告)号:EP2426146A2

    公开(公告)日:2012-03-07

    申请号:EP11185989.8

    申请日:2008-12-08

    IPC分类号: C07K16/24

    摘要: There is provided an anti-human IL-21 monoclonal antibody comprising: (a) a heavy chain region comprising: (i) a heavy chain variable region CDR1 comprising SEQ ID NO: 63; (ii) a heavy chain variable region CDR2 comprising SEQ ID NO: 65; and (iii) a heavy chain variable region CDR3 comprising SEQ ID NO: 67; and (b) a light chain region comprising: (i) a light chain variable region CDR1 comprising SEQ ID NO: 71; (ii) a light chain variable region CDR2 comprising SEQ ID NO: 73; and (iii) a light chain variable region CDR3 comprising SEQ ID NO: 75. There is also provided a hybridoma designated 366.328.10, wherein the hybridoma is deposited with the American Type Culture Collection having the ATCC Patent Deposit Designation PTA-8789.

    摘要翻译: 提供抗人IL-21单克隆抗体,其包含:(a)重链区,其包含:(i)包含SEQ ID NO:63的重链可变区CDR1; (ii)包含SEQ ID NO:65的重链可变区CDR2; 和(iii)包含SEQ ID NO:67的重链可变区CDR3; 和(b)轻链区,其包含:(i)包含SEQ ID NO:71的轻链可变区CDR1; (ii)包含SEQ ID NO:73的轻链可变区CDR2; 还提供了包含SEQ ID NO:75的轻链可变区CDR3。还提供了称为366.328.10的杂交瘤,其中杂交瘤保藏在具有ATCC专利保藏号PTA-8789的美国典型培养物保藏中心。

    Compositions and methods for inhibiting PDGFRBETA and VEGF-A
    5.
    发明公开
    Compositions and methods for inhibiting PDGFRBETA and VEGF-A 审中-公开
    Zusammensetzungen und Verfahren zur Hemmung von PDGFR-β和VEGF-A

    公开(公告)号:EP2604280A3

    公开(公告)日:2013-10-16

    申请号:EP13159556.3

    申请日:2009-03-27

    摘要: There is provided an isolated antibody that binds to the extracellular domain of PDGFRβ and neutralizes PDGFRβ activity, said antibody comprising a V L domain comprising CDRs LCDR1, LCDR2, and LCDR3 and a V H domain comprising CDRs HCDR1, HCDR2, and HCDR3, wherein:
    LCDR1 has the amino acid sequence shown in SEQ ID NO: 433, optionally the amino acid sequence shown in SEQ ID NO: 443;
    LCDR2 has the amino acid sequence shown in SEQ ID NO: 434;
    LCDR3 has the amino acid sequence shown in SEQ ID NO: 435, optionally the amino acid sequence shown in SEQ ID NO: 444;
    HCDR1 has the amino acid sequence shown in SEQ ID NO: 436, optionally the amino acid sequence shown in SEQ ID NO: 445;
    HCDR2 has the amino acid sequence shown in SEQ ID NO: 437;
    HCDR3 has an amino acid sequence selected from the group consisting of SEQ ID NOs: 438-442

    摘要翻译: 提供了结合PDGFR2的细胞外结构域并中和PDGFR2活性的分离的抗体,所述抗体包含包含CDR1 LCDR1,LCDR2和LCDR3的VL结构域和包含CDR HCDR1,HCDR2和HCDR3的VH结构域,其中:LCDR1具有 SEQ ID NO:433所示的氨基酸序列,任选地SEQ ID NO:443所示的氨基酸序列; LCDR2具有SEQ ID NO:434所示的氨基酸序列; LCDR3具有SEQ ID NO:435所示的氨基酸序列,任选地SEQ ID NO:444所示的氨基酸序列; HCDR1具有SEQ ID NO:436所示的氨基酸序列,任选地是SEQ ID NO:445所示的氨基酸序列; HCDR2具有SEQ ID NO:437所示的氨基酸序列; HCDR3具有选自SEQ ID NO:438-442的氨基酸序列

    Compositions and methods for inhibiting PDGFRBETA and VEGF-A
    6.
    发明公开
    Compositions and methods for inhibiting PDGFRBETA and VEGF-A 审中-公开
    用于抑制PDGFRBETA和VEGF-A的组合物和方法

    公开(公告)号:EP2604280A2

    公开(公告)日:2013-06-19

    申请号:EP13159556.3

    申请日:2009-03-27

    摘要: There is provided an isolated antibody that binds to the extracellular domain of PDGFRβ and neutralizes PDGFRβ activity, said antibody comprising a V L domain comprising CDRs LCDR1, LCDR2, and LCDR3 and a V H domain comprising CDRs HCDR1, HCDR2, and HCDR3, wherein:
    LCDR1 has the amino acid sequence shown in SEQ ID NO: 433, optionally the amino acid sequence shown in SEQ ID NO: 443;
    LCDR2 has the amino acid sequence shown in SEQ ID NO: 434;
    LCDR3 has the amino acid sequence shown in SEQ ID NO: 435, optionally the amino acid sequence shown in SEQ ID NO: 444;
    HCDR1 has the amino acid sequence shown in SEQ ID NO: 436, optionally the amino acid sequence shown in SEQ ID NO: 445;
    HCDR2 has the amino acid sequence shown in SEQ ID NO: 437;
    HCDR3 has an amino acid sequence selected from the group consisting of SEQ ID NOs: 438-442

    摘要翻译: 提供了与PDGFRβ的胞外结构域结合并中和PDGFRβ活性的分离的抗体,所述抗体包含含有CDR LCDR1,LCDR2和LCDR3的VL结构域和包含CDR HCDR1,HCDR2和HCDR3的VH结构域,其中:LCDR1具有 SEQ ID NO:433所示的氨基酸序列,任选的SEQ ID NO:443所示的氨基酸序列; LCDR2具有SEQ ID NO:434所示的氨基酸序列; LCDR3具有SEQ ID NO:435所示的氨基酸序列,任选地SEQ ID NO:444所示的氨基酸序列; HCDR1具有SEQ ID NO:436中所示的氨基酸序列,任选地SEQ ID NO:445中所示的氨基酸序列; HCDR2具有SEQ ID NO:437所示的氨基酸序列; HCDR3具有选自SEQ ID NO:438-442的氨基酸序列