Compositions and methods for inhibiting PDGFRBETA and VEGF-A
    2.
    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
    3.
    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