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    Home > Biochemistry News > Biotechnology News > More than half of the patients' skin symptoms improved by more than 75%. Eli Lilly's eczema antibody therapy reached the phase 3 clinical endpoint

    More than half of the patients' skin symptoms improved by more than 75%. Eli Lilly's eczema antibody therapy reached the phase 3 clinical endpoint

    • Last Update: 2021-09-05
    • Source: Internet
    • Author: User
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    On August 16, 2021, Eli Lilly and Company announced that lebrikizumab, a monoclonal antibody therapy targeting IL-13, has reached the primary endpoint in two pivotal Phase 3 clinical trials ADvocate 1 and ADvocate 2 And all key secondary endpoints


    Atopic dermatitis, also known as eczema, is a chronic inflammatory skin disease caused by skin barrier dysfunction and immune response disorders


    Lebrikizumab is an innovative monoclonal antibody drug that can bind IL-13 with high affinity and high specificity, thereby preventing the formation of IL-13Rα1/IL-4Rα complex and inhibiting the receptor complex-mediated Signal pathway


    ▲The mechanism of action of Lebrikizumab and other antibody therapies targeting IL-4 and IL-13 signaling pathways (picture source: reference [2])

    In terms of safety, during the initial 16-week control period, the incidence of adverse events (AE) and serious AEs after lebrikizumab treatment was consistent with previous studies


    Reference materials:

    [1] Lilly's lebrikizumab significantly improved skin clearance and itch in people with moderate-to-severe atopic dermatitis in two Phase 3 trials.


    [2] Moyle et al.


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