echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Immunology News > ARD: Anifrolumab efficacy and safety according to type I interferon gene signature and clinical subgroups in SLE patients: a post hoc analysis of pooled data from two phase III trials

    ARD: Anifrolumab efficacy and safety according to type I interferon gene signature and clinical subgroups in SLE patients: a post hoc analysis of pooled data from two phase III trials

    • Last Update: 2022-04-23
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    OBJECTIVE: Systemic lupus erythematosus (SLE) is a heterogeneous disease in which patient demographic and clinical characteristics correlate with disease severity and response to treatment
    .


    Anifrolumab , a human monoclonal antibody that binds to type I interferon receptor subunit 1 , has demonstrated efficacy and an acceptable safety profile in patients with moderate-to-severe SLE in Phase III clinical trials .


    OBJECTIVE: Systemic lupus erythematosus (SLE) is a heterogeneous disease in which patient demographic and clinical characteristics correlate with disease severity and response to treatment


    Methods: We performed a post hoc analysis of pooled data from the 52 - week phase III TULIP-1/TULIP-2 placebo-controlled trial of intravenous anifrolumab in patients withmoderate-to-severe SLE .
    Outcomes were assessed in predefined subgroups: IFNGS (high / low), age, sex, body mass index, ethnicity, geographic region, age at onset, glucocorticoid use, disease activity, and serological markers .

    RESULTS: In pooled data, patients received anifrolumab 300 mg (360/726) or placebo (366/726) ; 82.


    6% were IFNGS high


    RESULTS: In pooled data, patients received anifrolumab 300 mg (360/726) or placebo (366/726) ; 82.
    6% were IFNGS high


    Conclusions: Overall, this study supports the consistent efficacy and safety of anifrolumab in a range of patients with moderate to severe SLE .
    In a few subgroups, the small sample size limited consistent efficacy and safety among patients .
    Conclusions on whether anifrolumab treatment is beneficial .

     

    Source: Vital EM, Merrill JT, Morand EF , et al.


    Anifrolumab efficacy and safety by type I interferon gene signature and clinical subgroups in patients with SLE: post hoc analysis of pooled data from two phase III trials.
    Annals of the Rheumatic Diseases  Published Online First: 25 March 2022.
    doi: 10.


    Vital EM, Merrill JT, Morand EF , et al.
    , et al.
    Anifrolumab efficacy and safety by type I interferon gene signature and clinical subgroups in patients with SLE: post hoc analysis of pooled data from two phase III trials.
    Annals of the Rheumatic Diseases  Annals of the Rheumatic Diseases  Published Online First: 25 March 2022.
    doi: 10.
    1136/annrheumdis-2021-221425 Leave a comment here
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.