AUTHOR=Zhu Ke-Wei 

TITLE=Efficacy and safety evaluation of Azvudine in the prospective treatment of COVID-19 based on four phase III clinical trials

JOURNAL=Frontiers in Pharmacology

VOLUME=Volume 14 - 2023

YEAR=2023

URL=https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2023.1228548

DOI=10.3389/fphar.2023.1228548

ISSN=1663-9812

ABSTRACT=Azvudine (FNC) is a synthetic nucleoside analog used to treat adult patients suffering from human immunodeficiency virus-1 (HIV-1) infection with high viral load. After phosphorylation, Azvudine inhibits RNA-dependent RNA polymerase (RdRp), leading to discontinuation of RNA chain synthesis in viruses. In addition, Azvudine is the first dual-target nucleoside oral drug worldwide to simultaneously target reverse transcriptase and viral infectivity factors in the treatment of HIV infection. On August 9, 2022, Azvudine was included into the Guidelines for the Diagnosis and Treatment of Coronavirus Disease 2019 (version ninth) issued by the National Health Commission and National Administration of Traditional Chinese Medicine. The recommended oral dose of Azvudine for the treatment of moderate coronavirus disease 2019 (COVID-19) is 5 mg once daily, and the duration of Azvudine treatment should not exceed 14 days. Four phase Ⅲ clinical trials were performed during 2020 – 2022 to evaluate the efficacy and safety of Azvudine in the treatment of COVID-19. The results revealed that Azvudine could reduce nucleic acid negative conversion (NANC) time, viral load, and time to improvement in clinical condition in patients with moderate COVID-19. In addition, Azvudine exhibited good safety and well tolerance. Thereafter, Azvudine was included into the Chinese guideline and expert consensus for the treatment of COVID-19, and was highly approbated. Meanwhile, Azvudine was included into the Chinese guideline for HIV infection.