echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medicines Company News > ACC008 Phase III clinical trial completed the enrolment of clinical subjects

    ACC008 Phase III clinical trial completed the enrolment of clinical subjects

    • Last Update: 2022-05-21
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com

    Recently, Aidi Pharmaceuticals (stock code: SH.
    688488) announced in its annual report that its ainovirine-based anti-AIDS three-in-one compound single-tablet preparation ACC008 (ANV 150mg + TDF 300mg + 3TC 300mg) targets HIV.
    The phase III clinical trial of infected patients has completed the enrollment of 762 clinical subjects
    .
    The trial adopted a multi-center, randomized, double-blind, double-dummy, positive parallel-controlled, non-inferiority trial, and included 762 clinical subjects who had been diagnosed with HIV infection and were carried out in 10 well-known AIDS clinical trial institutions across the country.
    A head-to-head test with the imported original research drug Icogen Bacterial Tablets (trade name: Jie Fu Kang?)
    .
    The phase III clinical study of ACC008 tablets is the first phase III clinical study of the first-line treatment regimen for HIV-experienced patients in China.
    The core drug in the ACC008 formula, ainovirine, can significantly reduce central nervous system adverse reactions compared with existing similar drugs
    .
    At the same time, ACC008 completed the bioequivalence trial in March 2021, and the new drug marketing application for HIV-infected patients was accepted by NMPA in May 2021 and is currently under review
    .
    The combination regimen and drug selection of ACC008 are in line with the international trend.
    Patients only need to take 1 tablet per day and do not need to take other anti-AIDS drugs, which helps to reduce the burden of patients taking medication, increase compliance, and reduce the occurrence of drug resistance
    .
    If the product successfully completes the clinical research and is approved for marketing, it will help provide a new choice for domestic HIV-infected patients to keep pace with the international community and meet the growing medical needs of the domestic public
    .
    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.