Safety, Pharmacokinetics, and Antiviral Activity of AT-527, a Novel Purine Nucleotide Prodrug, in Hepatitis C Virus-Infected Subjects with or without Cirrhosis

Author:

Berliba Elina1,Bogus Maxim1,Vanhoutte Frédéric2,Berghmans Pieter-Jan2,Good Steven S.3,Moussa Adel3,Pietropaolo Keith3,Murphy Robert L.34,Zhou Xiao-Jian3,Sommadossi Jean-Pierre3

Affiliation:

1. ARENSIA Exploratory Medicine, Republican Clinical Hospital, Chisinau, Moldova

2. SGS Life Sciences, Antwerp, Belgium

3. Atea Pharmaceuticals, Inc., Boston, Massachusetts, USA

4. Northwestern University, Chicago, Illinois, USA

Abstract

AT-527 is a novel modified guanosine nucleotide prodrug inhibitor of the hepatitis C virus (HCV) NS5B polymerase, with increased in vitro antiviral activity compared to sofosbuvir and a highly differentiated favorable preclinical profile compared to other anti-HCV nucleoside/nucleotide analogs.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference27 articles.

1. World Health Organization. 2017. Global hepatitis report, 2017. World Health Organization, Geneva, Switzerland. https://apps.who.int/iris/bitstream/handle/10665/255016/9789241565455-eng.pdf;jsessionid=8EB397C58B3837AB5F66A2E8C53A8718?sequence=1. Accessed 23 September 2019.

2. AASLD-IDSA. 2019. Recommendations for testing managing and treating hepatitis C. American Association for the Study of Liver Diseases and Infectious Diseases Society of America. http://www.hcvguidelines.org. Accessed 23 September 2019.

3. Closing the Gap: The Challenges of Treating Hepatitis C Virus Genotype 3 Infection

4. Is 3 the new 1: perspectives on virology, natural history and treatment for hepatitis C genotype 3

5. Glecaprevir/pibrentasvir for hepatitis C virus genotype 3 patients with cirrhosis and/or prior treatment experience: A partially randomized phase 3 clinical trial

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