echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Immunology News > JAMA: The effect of costimulation blockade of abatacept on patients with moderate to severe plaque psoriasis after discontinuation of Uselumumab PAUSE randomized clinical trial

    JAMA: The effect of costimulation blockade of abatacept on patients with moderate to severe plaque psoriasis after discontinuation of Uselumumab PAUSE randomized clinical trial

    • Last Update: 2021-11-02
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    The recurrence of psoriasis may involve the compensatory T cell activation pathway in the case of blocking CD28-CD80/CD86 with abatacept
    .


    To determine whether the use of abatacept for costimulatory signal blockade can prevent the recurrence of psoriasis after the discontinuation of Uselnumumab


    experimental design:

    Treatment of psoriasis with abatacept and usnumab: The Efficacy Study (PAUSE), a parallel-designed, double-blind, placebo-controlled randomized clinical trial conducted at 10 locations in the United States and Canada
    .


    Participant recruitment started on March 19, 2014 and ended on April 11, 2016


    Participant

     

    Those patients who responded to ustekinumab in the 12th week were randomly assigned 1:1 to continue ustekinumab group (ustekinumab group) or switch to abatacept group (abatacept group) )
    .


    Treatment was stopped at week 39, and participants were followed up until week 88 for recurrence of psoriasis


     

    Clinical intervention:

    Participants received subcutaneous injections of Uselnumumab (45 mg per dose for patients ≤100 kg; 90 mg per dose for patients> 100 kg) at week 0 and week 4
    .


    Participants who were randomly assigned to the abatacept group at week 12 received subcutaneous abatacept at 125 mg per week from week 12 to week 39, and received ustekinumab placebo at week 16 and week 28


     

    Experimental endpoint: The primary endpoint is the proportion of participants with psoriasis recurrence between week 12 and week 88 (loss of initial psoriasis area and severity index improvement ≥50%)
    .


    Secondary endpoints included time to psoriasis recurrence, proportion of participants with psoriasis recurring between weeks 12 and 40, and adverse events


     

    Results: A total of 108 participants (mean [SD] age, 46.
    1 [12.
    1] years; 73 [67.
    6%] men) received open-label ustekinumab treatment; 91 people were randomized to receive blind treatment
    .


    Participants in the abatacept group and ustekinumab group had similar relapse rates between weeks 12 and 88 (41 out of 45 people [91.


     

    Conclusion: This parallel-designed, double-blind randomized clinical trial found that abatacept does not prevent psoriasis recurrence that occurs after the withdrawal of uxinuzumab , because it does not completely block the pathogenic psoriasis molecule that causes the recurrence way

    Prevent leaving a message 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.