echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Active Ingredient News > Antitumor Therapy > GnRH antagonist linzagolix treats uterine fibroids, with positive results in Phase 3 studies

    GnRH antagonist linzagolix treats uterine fibroids, with positive results in Phase 3 studies

    • Last Update: 2020-07-14
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com
    ObsEva SA announced data from the 3rd Phase study (PRIMROSE 1 and 2), which evaluated the effectiveness and safety of the GnRH (gonadotropin-releasing hormone) an tagane Yselty (linzagolix) for the treatment of large period bleeding in patients with uterine fibroidsPRIMROSE 1 reached the primary endpoint at week 24, and the amount of menstrual bleeding was significantly reduced in women receiving linzagolix compared to the placebo (s.80 mL, a decrease of 50% compared to the baseline)New data from PRIMROSE 2 show that 52 weeks of treatment with linzagolix provides consistent efficacy and is well toleratedin two studies, patients treated with linzagolix had statistically significant improvements in many clinically relevant secondary endpoints, including pain reduction, improved anemia, and quality of lifeProfessor Hugh Taylor, of yale, said: "Women with uterine fibroids experience pain and discomfort due to menstrual haemorrhage, and a large number of patients who do not accept or wish to avoid hormone replacement therapy, requiring new and effective treatments that can provide lasting relief to symptoms." These results show that linzagolix can effectively control bleeding, reduce pain associated with fibroids and improve anemiaThis could be a long-awaited new treatment to meet currently unmet needs"
    ObsEva is now preparing to submit regulatory documents to the European DrugAdministration(EMA) and the U.SFood and Drug Administration (
    FDA), which are expected to be filed in the fourth quarter of 2020 and January 2021, respectivelyData from the entire clinical trial program will be presented to an upcoming scientific conference
    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.