echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical Research Articles > FDA approves blockbuster Dupixent extension for treatment of patients aged 12-17 with severe asexual dermatitis

    FDA approves blockbuster Dupixent extension for treatment of patients aged 12-17 with severe asexual dermatitis

    • Last Update: 2020-06-10
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    amyritis, also known as eczema, is a common chronic inflammatory skin diseaseIts clinical symptoms include dry skin, redness and itchingA rash in patients with moderate lytosis may cover most of the body's skin, leading to severe, persistent itchingSevere itching can be a heavy burden on the patientToday, the U.Sfda(http:// announcedthat it has approved the extension of dupixent, a heavy-duty drug developed jointly by Regeneron Pharmaceuticals(http://and Sanofi, to treat patients between the ages of 12 and 17 with severe asexual itistThe symptoms of these patients were not fully controlled after receiving prescription treatment for external use, or they were not suitable for the use of topical medicationsDupixent can be used as a single-drug therapy or in combination with external corticosteroidsIt is estimated that the number of adolescent patients with isotrophic dermatitis is half that of adult patients, and this approval means that the number of patients treated with acursion in Dupixent has increased by 50 per centAbout Dupixent
    Dupixent is a targeted biologicthe that inhibits both IL-4 and IL-13 signaling pathwaysIL-4 and IL-13 play a key role in type 2 inflammatory responses, which are important mechanisms for leading to adhesion dermatitis and other severe allergic diseasesDupixent has received FDA approval to treat adult patients with severe dermatitisIt has been approved by the FDA for breakthrough therapy for the treatment of adolescent patients with severe dermatitisThis approval is based on Dupixent's performance in the critical Phase 3 ClinicalTrial(http://, and after 16 weeks of treatment, the average improvement in eczema area and severe index (EASI) compared to baseline in patients in the Dupixent treatment group was 66% compared to baseline and 24% in the control groupThe number of patients treated with Dupixent for skin symptoms disappeared completely or almost completely more than 10 times in the control groupDupixent therapy also significantly reduced the patient's itching symptoms, and the number of patients with itching symptoms significantly reduced was 7 times that of the control group
    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.