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    • 1. 发明申请
    • TREATMENT OF ALZHEIMER'S DISEASE SUBPOPULATIONS WITH POOLED IMMUNOGLOBULIN G
    • 治疗阿尔茨海默病患者血液中游离脂肪酸G
    • WO2014182631A1
    • 2014-11-13
    • PCT/US2014/036848
    • 2014-05-05
    • BAXTER INTERNATIONAL INC.BAXTER HEALTHCARE SA
    • GELMONT, David, M.SINGER, JuliaFRITSCH, SandorSCHWARZ, Hans-Peter
    • A61K39/00
    • C07K16/18A61K38/47A61K39/39516A61K2039/505C07K16/06C07K16/065G01N33/6896
    • The present invention provides, among other aspects, methods for the treatment of Alzheimer's disease in a subject in need thereof, the method including administration of a therapeutically effective amount of a pooled human immunoglobulin G (IgG) composition to a subject with moderately severe Alzheimer's disease, a subject carrying an ApoE4 allele, or both, where the amount of pooled human IgG is from 300 mg/kg to 800 mg/kg body weight of the subject per two week period, and where the amount is administered in one or more doses during the two week period after initiation of a therapeutic regimen. Also provided, are methods for selecting a treatment regimen for a subject with Alzheimer's disease, including diagnosing the severity of the Alzheimer's disease, determining if the subject carries an APOE4 allele, or both, and assigning a treatment regimen including administration of pooled human immunoglobulin G and/or an anti-beta amyloid monoclonal antibody.
    • 除其他方面外,本发明还提供了在有需要的受试者中治疗阿尔茨海默氏病的方法,所述方法包括将治疗有效量的合并的人免疫球蛋白G(IgG)组合物给予具有中等严重阿尔茨海默病的受试者 ,携带ApoE4等位基因或两者的受试者,其中合并的人IgG的量为每两周一次的受试者体重为300mg / kg至800mg / kg,并且其中以一个或多个剂量 在开始治疗方案后的两周期间。 还提供了用于选择阿尔茨海默氏病患者的治疗方案的方法,包括诊断阿尔茨海默氏病的严重程度,确定受试者是否携带APOE4等位基因,或两者,以及分配治疗方案,包括给予合并的人免疫球蛋白G 和/或抗β淀粉样蛋白单克隆抗体。