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    Home > Biochemistry News > Biotechnology News > Preliminary clinical trial results of innovative gene therapy to treat fatal childhood immunodeficiency are positive

    Preliminary clinical trial results of innovative gene therapy to treat fatal childhood immunodeficiency are positive

    • Last Update: 2021-11-01
    • Source: Internet
    • Author: User
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    A few days ago, Rocket Pharmaceuticals announced that its research gene therapy RP-L201 has obtained positive interim data in a phase 1/2 clinical trial for the treatment of leukocyte adhesion deficiency type I (LAD-I)


    The clinical manifestations of type I leukocyte adhesion deficiency are delayed umbilical cord shedding, repeated soft tissue infections and chronic periodontitis


    RP-L201 is an in vitro autologous hematopoietic stem cell gene therapy based on lentiviral vector


    This interim data comes from 7 patients with severe LAD-I, whose CD18 expression is less than 2%


    Reference materials:

    [1] Rocket Pharmaceuticals Announces Positive Clinical Data from RP-L201 Trial for the Treatment of LAD-I at the 28th Annual Congress of the European Society of Gene & Cell Therapy (ESGCT).


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