Neuroprotection in Demyelinating Diseases
    51.
    发明申请
    Neuroprotection in Demyelinating Diseases 审中-公开
    神经保护脱髓鞘疾病

    公开(公告)号:US20130287732A1

    公开(公告)日:2013-10-31

    申请号:US13850240

    申请日:2013-03-25

    Abstract: Methods of treating neurological disorders, e.g., those characterized by demyelination and/or axonal loss (e.g., MS), are provided. The methods comprise administration of a therapeutically effective amount of at least one compound of Formula I: wherein R1 and R2 are independently selected from OH, O−, and (C1-6)alkoxy, or a pharmaceutically acceptable salt thereof; and either glatiramer acetate or interferon-beta.

    Abstract translation: 提供治疗神经系统疾病的方法,例如由脱髓鞘和/或轴突损失(例如MS)表征的那些。 所述方法包括施用治疗有效量的至少一种式I化合物:其中R 1和R 2独立地选自OH,O-和(C 1-6)烷氧基,或其药学上可接受的盐; 和醋酸格拉默或干扰素-β。

    METHODS OF USING A FIXED DOSE OF A CLOTTING FACTOR
    56.
    发明申请
    METHODS OF USING A FIXED DOSE OF A CLOTTING FACTOR 审中-公开
    使用固定因子的固定剂量的方法

    公开(公告)号:US20160296607A1

    公开(公告)日:2016-10-13

    申请号:US14436667

    申请日:2013-10-18

    Inventor: Haiyan JIANG

    Abstract: The present invention provides methods of administering a clotting factor by a fixed dosing regimen; methods of reducing, ameliorating, or preventing one or more symptoms of a bleeding disease or disorder; and a kit comprising a dotting factor useful for a fixed dosing regimen. While plasma-derived and recombinant clotting factor products allow hemophilia patients to live longer and healthier, hemophilia still remains one of the most costly and complex conditions to manage.

    Abstract translation: 本发明提供了通过固定给药方案施用凝血因子的方法; 降低,改善或预防出血性疾病或病症的一种或多种症状的方法; 以及包含可用于固定给药方案的点状因子的试剂盒。 虽然血浆来源和重组凝血因子产品允许血友病患者生活更健康,血友病仍然是最昂贵和复杂的管理条件之一。

    Nutrient monitoring and feedback control for increased bioproduct production
    59.
    发明授权
    Nutrient monitoring and feedback control for increased bioproduct production 有权
    营养监测和反馈控制,以增加生物产品生产

    公开(公告)号:US09212379B2

    公开(公告)日:2015-12-15

    申请号:US13659655

    申请日:2012-10-24

    Abstract: The present invention pertains to methods of increasing the efficiency of producing a bioproduct. In some embodiments, the method increases the quantity of a bioproduct produced, or decreases bioproduct production time, in a bioreactor cell culture producing the bioproduct, the method comprising, (a) intermittently or continuously analyzing the concentration of one or more nutrients in the bioreactor cell culture; and (b) adding to the bioreactor cell culture additional nutrient media when the concentration of the one or more nutrients is lower than a target value.

    Abstract translation: 本发明涉及提高生物制品生产效率的方法。 在一些实施方案中,该方法在产生生物产物的生物反应器细胞培养物中增加产生的生物产物的量或减少生物产物生产时间,该方法包括:(a)间歇地或连续地分析生物反应器中一种或多种营养物质的浓度 细胞培养; 和(b)当一种或多种营养素的浓度低于目标值时,向生物反应器细胞培养添加另外的营养培养基。

    Methods For Treating Tweak-Related Conditions
    60.
    发明申请
    Methods For Treating Tweak-Related Conditions 审中-公开
    治疗调整相关条件的方法

    公开(公告)号:US20150291688A1

    公开(公告)日:2015-10-15

    申请号:US14661391

    申请日:2015-03-18

    Abstract: The present invention provides methods and agents for the treatment of TWEAK-related conditions, including cardiac, liver, kidney, lung, adipose, skeletal, muscle, neuronal, bone and cartilage conditions. The invention also provides methods for identifying TWEAK agonists or antagonists for the treatment of TWEAK-related conditions. Additionally, the invention provides transgenic animals that express an exogenous DNA encoding a TWEAK polypeptide, or fragments, analogs, or muteins thereof, and methods for using such animals to identify TWEAK agonists or antagonists. The invention further provides methods for diagnosing a disease based on TWEAK expression. The invention also provides methods for affecting cellular differentiation of progenitor cells using TWEAK polypeptides, agonists, or antagonists.

    Abstract translation: 本发明提供了治疗TWEAK相关病症的方法和试剂,包括心脏,肝脏,肾脏,肺,脂肪,骨骼,肌肉,神经元,骨骼和软骨条件。 本发明还提供用于鉴定用于治疗TWEAK相关病症的TWEAK激动剂或拮抗剂的方法。 另外,本发明提供表达编码TWEAK多肽或其片段,类似物或突变蛋白的外源DNA的转基因动物,以及使用这些动物鉴定TWEAK激动剂或拮抗剂的方法。 本发明还提供了基于TWEAK表达来诊断疾病的方法。 本发明还提供了使用TWEAK多肽,激动剂或拮抗剂来影响祖细胞的细胞分化的方法。

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