COMPOSITIONS AND METHODS FOR INHIBITING VIRAL REPLICATION
    42.
    发明申请
    COMPOSITIONS AND METHODS FOR INHIBITING VIRAL REPLICATION 有权
    用于抑制病毒复制的组合物和方法

    公开(公告)号:US20080194512A1

    公开(公告)日:2008-08-14

    申请号:US11959936

    申请日:2007-12-19

    IPC分类号: A61K31/70 C07H21/04

    摘要: The present invention relates to a double-stranded ribonucleic acid (dsRNA) having a nucleotide sequence which is less that 30 nucleotides in length and which is substantially identical to at least a part of a 3′-untranslated region (3′-UTR) of a (+) strand RNA virus, such as HCV, as well as pharmaceutical compositions comprising the dsRNA, together with a pharmaceutically acceptable carrier. The pharmaceutical compositions are useful for treating infections and diseases caused by the replication or activity of the (+) strand RNA virus, as well as methods for inhibiting viral replication.

    摘要翻译: 本发明涉及具有长度小于30个核苷酸的核苷酸序列的双链核糖核酸(dsRNA),并且其基本上与3'非翻译区(3'-UTR)的至少一部分相同 (+)链RNA病毒,例如HCV,以及包含dsRNA的药物组合物,以及药学上可接受的载体。 药物组合物可用于治疗由(+)链RNA病毒的复制或活性引起的感染和疾病以及用于抑制病毒复制的方法。

    Compositions and methods for inhibiting viral replication
    44.
    发明授权
    Compositions and methods for inhibiting viral replication 有权
    用于抑制病毒复制的组合物和方法

    公开(公告)号:US07348314B2

    公开(公告)日:2008-03-25

    申请号:US10384512

    申请日:2003-03-07

    IPC分类号: A61K31/70 C07H21/04 C07H21/00

    摘要: The present invention relates to a double-stranded ribonucleic acid (dsRNA) having a nucleotide sequence which is less that 30 nucleotides in length and which is substantially identical to at least a part of a 3′-untranslated region (3′-UTR) of a (+) strand RNA virus, such as HCV, as well as pharmaceutical compositions comprising the dsRNA, together with a pharmaceutically acceptable carrier. The pharmaceutical compositions are useful for treating infections and diseases caused by the replication or activity of the (+) strand RNA virus, as well as methods for inhibiting viral replication.

    摘要翻译: 本发明涉及具有长度小于30个核苷酸的核苷酸序列的双链核糖核酸(dsRNA),并且其基本上与3'非翻译区(3'-UTR)的至少一部分相同 (+)链RNA病毒,例如HCV,以及包含dsRNA的药物组合物,以及药学上可接受的载体。 药物组合物可用于治疗由(+)链RNA病毒的复制或活性引起的感染和疾病以及用于抑制病毒复制的方法。

    RNAi Modulation of AHA and Therapeutic Uses Thereof
    45.
    发明申请
    RNAi Modulation of AHA and Therapeutic Uses Thereof 审中-公开
    AHA的RNAi调节及其治疗用途

    公开(公告)号:US20120142757A1

    公开(公告)日:2012-06-07

    申请号:US13343426

    申请日:2012-01-04

    摘要: The invention relates to a double-stranded ribonucleic acid (dsRNA) for inhibiting the expression of an Aha gene (Aha1 gene), comprising an antisense strand having a nucleotide sequence which is less that 30 nucleotides in length, generally 19-25 nucleotides in length, and which is substantially complementary to at least a part of an Aha gene. The invention also relates to a pharmaceutical composition comprising the dsRNA together with a pharmaceutically acceptable carrier; methods for treating diseases caused by Aha1 expression and the expression of an Aha gene using the pharmaceutical composition; and methods for inhibiting the expression of an Aha gene in a cell.

    摘要翻译: 本发明涉及用于抑制Aha基因(Aha1基因)表达的双链核糖核酸(dsRNA),其包含长度小于30个核苷酸的核苷酸序列的反义链,其长度通常为19-25个核苷酸 并且其与Aha基因的至少一部分基本上互补。 本发明还涉及包含dsRNA与药学上可接受的载体的药物组合物; 用于治疗由Aha1表达引起的疾病和使用该药物组合物表达Aha基因的方法; 以及抑制细胞中Aha基因表达的方法。