Antiviral Compositions And Methods Of Using The Same
    102.
    发明申请
    Antiviral Compositions And Methods Of Using The Same 审中-公开
    抗病毒组合物及其使用方法

    公开(公告)号:US20070259844A1

    公开(公告)日:2007-11-08

    申请号:US10561656

    申请日:2004-06-21

    申请人: Jong Kim

    发明人: Jong Kim

    摘要: Pharmaceutical compositions for and methods of preventing infection or treating an individual who has been identified as being infected with a Flavivirus, Pestivirus, picornovirus or coronavirus such as HCV, GB virus B, JEV, WNV, CSFV, BDV, BVDV, poliovirus, FMDV, or EMCV, comprising administering to the individual a therapeutically effective amount of one or more glucocorticoid receptor antagonist compounds, wherein said compound has steroidal structure are disclosed.

    摘要翻译: 用于预防感染或治疗被鉴定为感染黄病毒,瘟病毒,小细小病毒或冠状病毒如HCV,GB病毒B,JEV,WNV,CSFV,BDV,BVDV,脊髓灰质炎病毒,FMDV的个体的药物组合物和方法, 或EMCV,包括向个体施用治疗有效量的一种或多种糖皮质激素受体拮抗剂化合物,其中所述化合物具有甾体结构。

    Glycyrrhizin or derivatives thereof for for treating or preventing severe acute respiratory syndrome (sars)
    105.
    发明申请
    Glycyrrhizin or derivatives thereof for for treating or preventing severe acute respiratory syndrome (sars) 审中-公开
    甘草甜或其衍生物用于治疗或预防严重急性呼吸综合征(sars)

    公开(公告)号:US20070099855A1

    公开(公告)日:2007-05-03

    申请号:US10559495

    申请日:2004-06-07

    申请人: Jindrich Cinatl

    发明人: Jindrich Cinatl

    IPC分类号: A61K31/704

    摘要: The invention provides methods for preventing, treating, managing or ameliorating viral infections, in particular, Severe Acute Respiratory Syndrome (SARS). More specifically, the invention provides methods for preventing, treating, managing or ameliorating a SARS-associated coronavirus or one or more symptoms thereof by administering Glycyrrhizin and/or derivatives thereof The invention also provides methods for preventing, treating, managing or ameliorating a SARS-associated coronavirus or one or more symptoms thereof by administering Glycyrrhizin and/or a derivative thereof in combination with a prophylactic or therapeutic agent other than Glycyrrhizin or a derivative thereof.

    摘要翻译: 本发明提供了预防,治疗,治疗或改善病毒感染,特别是严重急性呼吸综合征(SARS)的方法。 更具体地,本发明提供了通过施用甘草甜素和/或其衍生物来预防,治疗,控制或改善与SARS相关的冠状病毒或其一种或多种症状的方法。本发明还提供了用于预防,治疗,控制或改善SARS- 通过与除甘草甜素或其衍生物以外的预防或治疗剂组合施用甘草甜素和/或其衍生物,与冠状病毒或其一种或多种症状相关。

    Combination therapy for treating alphavirus infection and liver fibrosis
    106.
    发明申请
    Combination therapy for treating alphavirus infection and liver fibrosis 审中-公开
    联合治疗甲病毒感染和肝纤维化

    公开(公告)号:US20070072181A1

    公开(公告)日:2007-03-29

    申请号:US10545864

    申请日:2004-02-26

    申请人: Lawrence Blatt

    发明人: Lawrence Blatt

    IPC分类号: C12Q1/70 C12Q1/68

    摘要: The present invention provides methods for treating alphavirus infections; methods of treating hepatitis C virus (HCV) infections; methods of treating West Nile virus infection; methods of reducing liver fibrosis; methods of increasing liver function in an individual suffering from liver fibrosis; methods of reducing the incidence of complications associated with HCV and cirrhosis of the liver; and methods of reducing viral load, or reducing the time to viral clearance, or reducing morbidity or mortality in the clinical outcomes, in patients suffering from viral infection. The methods generally involve administering effective amounts of an interferon receptor agonist and pirfenidone in combination therapy.

    摘要翻译: 本发明提供了治疗甲病毒感染的方法; 治疗丙型肝炎病毒(HCV)感染的方法; 治疗西尼罗病毒感染的方法; 减少肝纤维化的方法 增加肝纤维化患者肝功能的方法; 减少与HCV和肝硬化相关并发症发生率的方法; 以及在患有病毒感染的患者中减少病毒载量或减少病毒清除时间或减少临床结果的发病率或死亡率的方法。 所述方法通常涉及在组合疗法中施用有效量的干扰素受体激动剂和吡非尼酮。

    METHOD OF TREATING OR INHIBITING THE DEVELOPMENT OF BRAIN INFLAMMATION AND SEPSIS

    公开(公告)号:US20070054937A1

    公开(公告)日:2007-03-08

    申请号:US11555418

    申请日:2006-11-01

    申请人: Masako NOZAKI

    发明人: Masako NOZAKI

    IPC分类号: A61K31/47

    摘要: A leukotriene C4 and D4 antagonist is used to treat or inhibit brain inflammation and sepsis by acting to inhibit increased capillary permeability and white blood cell extravasation. Potential candidate compounds can be screened in a non-human mammal before or after administration of an inflammation inducing agent into the subarachnoid space by determining their ability to inhibit increased capillary permeability and white blood cell extravasation.