Remdesivir is an phosphoramidate prodrug that releases the monophosphate of nucleoside GS-441524 () into lung cells, thereby forming the bioactive triphosphate . , an analog of ATP, inhibits the SARS-CoV-2 RNA-dependent RNA polymerase replication and transcription of viral RNA. Strong clinical results for have prompted interest in oral approaches to generate . Here, we describe the discovery of a 5'-isobutyryl ester prodrug of (GS-5245, Obeldesivir, ) that has low cellular cytotoxicity and 3-7-fold improved oral delivery of in monkeys. Prodrug is cleaved presystemically to provide high systemic exposures of that overcome its less efficient metabolism to , leading to strong SARS-CoV-2 antiviral efficacy in an African green monkey infection model. Exposure-based SARS-CoV-2 efficacy relationships resulted in an estimated clinical dose of 350-400 mg twice daily. Importantly, all SARS-CoV-2 variants remain susceptible to , which supports development of as a promising COVID-19 treatment.
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http://dx.doi.org/10.1021/acs.jmedchem.3c00750 | DOI Listing |
Sci Transl Med
May 2024
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Despite the wide availability of several safe and effective vaccines that prevent severe COVID-19, the persistent emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) that can evade vaccine-elicited immunity remains a global health concern. In addition, the emergence of SARS-CoV-2 VOCs that can evade therapeutic monoclonal antibodies underscores the need for additional, variant-resistant treatment strategies. Here, we characterize the antiviral activity of GS-5245, obeldesivir (ODV), an oral prodrug of the parent nucleoside GS-441524, which targets the highly conserved viral RNA-dependent RNA polymerase (RdRp).
View Article and Find Full Text PDFScience
March 2024
Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, USA.
Obeldesivir (ODV, GS-5245) is an orally administered prodrug of the parent nucleoside of remdesivir (RDV) and is presently in phase 3 trials for COVID-19 treatment. In this work, we show that ODV and its circulating parent nucleoside metabolite, GS-441524, have similar in vitro antiviral activity against filoviruses, including Marburg virus, Ebola virus, and Sudan virus (SUDV). We also report that once-daily oral ODV treatment of cynomolgus monkeys for 10 days beginning 24 hours after SUDV exposure confers 100% protection against lethal infection.
View Article and Find Full Text PDFJ Med Chem
September 2023
Discovery Virology, Gilead Sciences Incorporated, 333 Lakeside Drive, Foster City, California 94404 United States.
Remdesivir is an phosphoramidate prodrug that releases the monophosphate of nucleoside GS-441524 () into lung cells, thereby forming the bioactive triphosphate . , an analog of ATP, inhibits the SARS-CoV-2 RNA-dependent RNA polymerase replication and transcription of viral RNA. Strong clinical results for have prompted interest in oral approaches to generate .
View Article and Find Full Text PDFbioRxiv
June 2023
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Despite the wide availability of several safe and effective vaccines that can prevent severe COVID-19 disease, the emergence of SARS-CoV-2 variants of concern (VOC) that can partially evade vaccine immunity remains a global health concern. In addition, the emergence of highly mutated and neutralization-resistant SARS-CoV-2 VOCs such as BA.1 and BA.
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