Peptides inhibiting plasma kallikrein for use in the treatment of ophthalmic disorders.
    6.
    发明授权
    Peptides inhibiting plasma kallikrein for use in the treatment of ophthalmic disorders. 有权
    血浆激肽释放的肽抑制剂用于眼科疾病的治疗中使用

    公开(公告)号:EP1854477B1

    公开(公告)日:2016-08-03

    申请号:EP07005182.6

    申请日:2007-03-13

    申请人: Dyax Corp.

    发明人: Belichard, Pierre

    IPC分类号: A61K38/55 A61P27/02

    CPC分类号: A61K38/57

    摘要: The present invention relates to compositions and methods for treating ophthalmic disorders of humans or animals. The present compositions and methods are highly suitable for intraocular administration into the interior of an eye and provide therapeutic effects to the eye as they are effective in stabilizing, enhancing and/or improving a patient's vision. More specifically, the present invention relates to compositions and methods for treating ophthalmic diseases or disorders with exudative, hemorrhagic and/or inflammatory conditions. Even more specifically, the present invention relates to compositions and methods for treating retinal diseases or disorders, and more specifically ophthalmic diseases or disorders related to impaired retinal vessel permeability and/or integrity.

    ANTIBODIES BINDING TO PHOSPHORYLCHOLINE (PC) AND/OR PC CONJUGATES
    10.
    发明公开
    ANTIBODIES BINDING TO PHOSPHORYLCHOLINE (PC) AND/OR PC CONJUGATES 审中-公开
    抗体结合磷酰胆碱(PC)和/或PC结合物

    公开(公告)号:EP2741770A1

    公开(公告)日:2014-06-18

    申请号:EP12821512.6

    申请日:2012-08-08

    IPC分类号: A61K39/00 A61K39/395

    摘要: The present disclosure relates to an antibody or antibody fragment capable of binding to phosphorylcholine and/or a phosphorylcholine conjugate, wherein the antibody or antibody fragment comprises a variable heavy chain (VH) domain and/or a variable light chain (VL) domain, and wherein (a) the VH domain comprises complementarity determining regions (CDRs) selected from the group consisting of: a CDR1 sequence having identity to the sequence of SEQ ID NO: 7; a CDR2 sequence having identity to the sequence of SEQID NO: 8; and a CDR3 sequence having identity to the sequence of SEQ ID NO: 9 or 10; and/or (b) the VL domain comprises CDRs selected from the group consisting of: a CDR4 sequence having identity to the sequence of SEQ ID NO: 11; a CDR5 sequence having identity to the sequence of SEQ ID NO: 12; a CDR6 sequence having identity to the sequence of SEQ ID NO: 13.