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    • 3. 发明申请
    • COMPOSITIONS AND METHODS FOR TREATMENT OF TRAUMA
    • 用于治疗创伤的组合物和方法
    • WO2009015087A2
    • 2009-01-29
    • PCT/US2008/070650
    • 2008-07-21
    • POTENTIA PHARMACEUTICALS, INC.FRANCOIS, CedricDESCHATELETS, PascalOLSON, Paul
    • FRANCOIS, CedricDESCHATELETS, PascalOLSON, Paul
    • A61K38/00A61K39/39C07K7/08
    • A61K38/12C12Q1/6883C12Q2600/106C12Q2600/136C12Q2600/156
    • The present invention features the use of a complement inhibitor, e.g., a compstatin analog for treating an individual who has suffered a severe injury. In some embodiments, the complement inhibitor may be administered within 24 hours following the injury and optionally also at later time points. The complement inhibitor may, for example, be administered prior to transporting the patient to a health care facility, during transport of the patient to a health care facility, or in the emergency department. Further provided are methods of selecting individuals for such therapy. Further provided are methods of identifying individuals at increased risk of poor outcome following trauma. In certain embodiments the methods comprise determining whether the genotype of the patient includes an allele of a polymorphism in or near a complement-related gene, wherein said allele is associated with risk of poor outcome following trauma.
    • 本发明的特征在于补体抑制剂例如坎普他汀类似物用于治疗遭受严重损伤的个体的用途。 在一些实施方案中,补体抑制剂可以在损伤后24小时内施用,并任选地在稍后的时间点施用。 例如,补体抑制剂可以在将患者运输到健康护理设施之前,在将患者运送到健康护理设施期间或在急诊室中进行施用。 还提供了选择用于这种治疗的个体的方法。 进一步提供了鉴定创伤后不良结局风险增加的个体的方法。 在某些实施方案中,所述方法包括确定患者的基因型是否在补体相关基因中或附近包含多态性的等位基因,其中所述等位基因与创伤后不良结果的风险相关。
    • 5. 发明申请
    • COMPOSITIONS AND METHODS FOR ENHANCING PHAGOCYTOSIS OR PHAGOCYTE ACTIVITY
    • 用于增强PHAGOCYTOSIS或PHAGOCYTE活性的组合物和方法
    • WO2005019429A2
    • 2005-03-03
    • PCT/US2004/027245
    • 2004-08-23
    • POTENTIA PHARMACEUTICALS, INC.FRANCOIS, CedricOLSON, PaulDESCHATELETS, PascalMACHIELS, Alec
    • FRANCOIS, CedricOLSON, PaulDESCHATELETS, PascalMACHIELS, Alec
    • C12N
    • B82Y5/00A61K47/544A61K47/62A61K47/6911A61K47/6913
    • The present invention provides a system for enhancing clearance or destruction of undesirable cells or noncellular molecular entities by tagging such cells or noncellular molecular entities with a marker that targets the cells or noncellular molecular entities for phagocytosis (phagocytic marker). The target cells can be, for example, endothelial cells, tumor cells, leukocytes, or virus-infected cells. In certain embodiments of the invention the tagging is accomplished by administering a composition comprising an antibody or ligand linked to the phagcytotic marker, wherein the antibody or ligand binds to a cell type specific marker present on or in the cell surface of a target cell. In preferred embodiments of the invention, the phagocytic marker comprises phosphatidylserine or a group derived from phosphatidylserine, thrombospondin-1, annexin I, or a derivative of any of these.
    • 本发明提供了一种用于通过用靶向细胞或非细胞分子实体进行吞噬作用(吞噬标记)的标记来标记这样的细胞或非细胞分子实体来增强不需要的细胞或非细胞分子实体的清除或破坏的系统。 靶细胞可以是例如内皮细胞,肿瘤细胞,白细胞或病毒感染的细胞。 在本发明的某些实施方案中,标记通过施用包含与噬菌体标记物连接的抗体或配体的组合物来实现,其中所述抗体或配体结合存在于靶细胞的细胞表面上或细胞表面的细胞类型特异性标志物。 在本发明的优选实施方案中,吞噬标记物包含磷脂酰丝氨酸或衍生自磷脂酰丝氨酸,血小板反应素-1,膜联蛋白I或其任何衍生物的基团。
    • 7. 发明申请
    • COMPOSITIONS AND METHODS FOR TREATMENT OF MACULAR DEGENERATION AND RELATED CONDITIONS
    • 用于治疗谷物变性和相关条件的组合物和方法
    • WO2006099330A2
    • 2006-09-21
    • PCT/US2006/008960
    • 2006-03-13
    • POTENTIA PHARMACEUTICALS, INC.DESCHATELETS, PascalFRANCOIS, Cedric
    • DESCHATELETS, PascalFRANCOIS, Cedric
    • A61K38/005A61L27/227
    • The present invention provides methods and compositions for treating and/or preventing age related macular degeneration and other conditions involving macular degeneration, ocular neovascularization, or ocular inflammation. The methods comprise administering a composition comprising a compound that is an antagonist of a G protein coupled receptor, e.g., the C5a receptor, to a subject in need of treatment or prevention of age-related macular degeneration or another condition involving macular degeneration or ocular neovascularization. The invention provides compositions comprising a compound that is an antagonist of a G protein coupled receptor linked either directly or indirectly to a moiety that binds to a component present on or at the surface of cell or noncellular molecular entity, e.g., a component present in the eye of a subject at risk of or suffering from age related macular degeneration or a related condition or choroidal neovascularization.
    • 本发明提供用于治疗和/或预防年龄相关性黄斑变性和涉及黄斑变性,眼新生血管形成或眼部炎症的其它病症的方法和组合物。 所述方法包括向需要治疗或预防年龄相关性黄斑变性的受试者或涉及黄斑变性或眼新生血管形成的另一种病症施用包含作为G蛋白偶联受体的拮抗剂的化合物(例如C5a受体)的组合物 。 本发明提供了包含化合物的组合物,其是G蛋白偶联受体的拮抗剂,其直接或间接地连接到与存在于细胞或非细胞分子实体上或其表面上的组分结合的部分,例如存在于 患有年龄相关性黄斑变性或相关病症或脉络膜新生血管形成危险的患者的眼睛。