Inhibition of angiogenesis
    2.
    发明授权
    Inhibition of angiogenesis 有权
    抑制血管发生

    公开(公告)号:US08470607B2

    公开(公告)日:2013-06-25

    申请号:US12933638

    申请日:2008-09-17

    摘要: The present invention is directed to novel methods of inhibiting angiogenesis using chlorotoxin agents. In some embodiments, the inventive methods include intravenous, intraocular, intravitreal, subjunctival injection, and/or topical administration of a chlorotoxin agent that may or may not be labeled. In some embodiments, the inventive methods allow treatment and/or amelioration of ocular diseases characterized by neovascularization, such as wet macular degeneration. In some embodiments, neovascularization is inhibited and/or newly formed vessels are caused to regress.

    摘要翻译: 本发明涉及使用氯毒素试剂抑制血管发生的新方法。 在一些实施方案中,本发明的方法包括静脉内,眼内,玻璃体内,结膜下注射和/或局部施用可能标记或可能不标记的氯毒素试剂。 在一些实施方案中,本发明的方法允许治疗和/或改善以新血管形成为特征的眼部疾病,例如湿性黄斑变性。 在一些实施方案中,新血管形成被抑制并且/或新形成的血管被引起退化。

    CHLOROTOXINS AS DRUG CARRIERS
    7.
    发明申请
    CHLOROTOXINS AS DRUG CARRIERS 审中-公开
    氯霉素作为药物载体

    公开(公告)号:US20110091380A1

    公开(公告)日:2011-04-21

    申请号:US12672069

    申请日:2008-08-07

    CPC分类号: A61K47/6415

    摘要: The present invention relates to the use of a toxin moiety (e.g., a chlorotoxin moiety) as a carrier for therapeutic agents, e.g., therapeutic agents that require intracellular uptake to exert their effects. For example, in some embodiments, the present invention provides conjugates comprising a toxin (e.g., a chlorotoxin) moiety and an anti-cancer moiety and methods for using such conjugates to increase cellular uptake and/or increase specificity for cancer cells of the anti-cancer drug. In some embodiments, the present invention provides conjugates comprising a toxin moiety (e.g., a chlorotoxin moiety) and a nucleic acid agent. Also provided are methods of treatment involving administration of such conjugates, and pharmaceutical compositions and kits useful for carrying out such methods of treatment.

    摘要翻译: 本发明涉及毒素部分(例如,氯毒素部分)作为治疗剂的载体的用途,例如需要细胞内吸收发挥其作用的治疗剂。 例如,在一些实施方案中,本发明提供了包含毒素(例如,氯毒素)部分和抗癌部分的缀合物以及使用这种缀合物增加细胞摄取和/或增加抗 - 癌症药物。 在一些实施方案中,本发明提供了包含毒素部分(例如,氯毒素部分)和核酸试剂的缀合物。 还提供了涉及施用这种缀合物的治疗方法,以及可用于实施这些治疗方法的药物组合物和试剂盒。