top of page

China Approves Oral pill COVID Antiviral-Azvudine

Writer's picture: Sharan MuruganSharan Murugan

Earlier Monday, China's drug regulator granted conditional approval for an HIV drug to treat COVID-19. This is the first oral antiviral made in China, Azvudine, developed by Genuine Biotech.


Genuine Biotech is headquartered in Pingdingshan, and applied for regulatory approval earlier this month. According to a company announcement, 40 percent of COVID-19 patients who were given Azvudine for a week showed improvement, compared to 11% of placebo patients. The third and late-stage clinical trials show that the oral medication is safe, can improve clinical conditions of patients and inhibit the virus within about five days.

So how does Azvudine work?

Most antivirals target two SARS-CoV-2 proteins that are essential for replication, a polymerase and a protease. Azvudine tricks the virus’s polymerase into incorporating the drug into its RNA, which stops the virus from replicating.


Another Chinese-made oral antiviral, VV116, is in the final stages of development, and another dozen are in various stages of development.



The developers of VV116, Shanghai Junshi Biosciences, plan to seek regulatory approval soon. VV116 is essentially a pill version of the intravenous drug remdesivir, made by Gilead Sciences in Foster City, California, and the first drug approved by the US Food and Drug Administration for treating COVID-19.



Comments


I Sometimes Send Newsletters

Thanks for submitting!

  • LinkedIn
  • Facebook
  • Twitter
  • Instagram

DISCLAIMER

The views expressed in this publication do not necessarily reflect the views of any guidance of government, health authority, it's purely my understanding. This Blog/Web Site is made available by a regulatory professional, is for educational purposes only as well as to give you general information and a general understanding of the pharmaceutical regulations, and not to provide specific regulatory advice. By using this blog site you understand that there is no client relationship between you and the Blog/Web Site publisher. The Blog/Web Site should not be used as a substitute for competent pharma regulatory advice and you should discuss from an authenticated regulatory professional in your state.  We have made every reasonable effort to present accurate information on our website; however, we are not responsible for any of the results you experience while visiting our website and request to use official websites.

bottom of page