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Preclinical characterization of an intravenous coronavirus 3CL protease inhibitor for the potential treatment of COVID19

Authors :
Heather Eng
Annaliesa S. Anderson
Norimitsu Shirai
Brandon J. Anson
James Logue
Stuart Weston
Marisa McGrath
Martyn D. Ticehurst
Rebecca E. O’Connor
Michelle Rossulek
Martin Pettersson
Matthew N O' Brien
Jean G. Sathish
Matthew B. Frieman
Emi Kimoto
Jun Wang
R. Scott Obach
Emily I. Chen
Robert Haupt
Yuao Zhu
Thomas F. Rogers
Andrew D. Mesecar
Suman Luthra
Adolfo García-Sastre
Dafydd R. Owen
Rhys M. Jones
Eugene P. Kadar
Chunlong Ma
Rob Kania
Lisa Aschenbrenner
Arnab K. Chatterjee
Charlotte Moira Norfor Allerton
Joseph John Binder
Kevin Ogilvie
Holly L. Hammond
Nathan Beutler
Claire M. Steppan
Jennifer Hammond
Stephen Noell
Romel Rosales
Robert M. Hoffman
Lillis Jonathan Richard
Matthew R. Reese
Stephen W. Mason
Dan Arenson
Malina A. Bakowski
Lawrence W. Updyke
Lorraine F. Lanyon
Kris M. White
Emma K. Lendy
Melanie G. Kirkpatrick
Britton Boras
Source :
bioRxiv, Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
Publication Year :
2021

Abstract

COVID-19 caused by the SARS-CoV-2 virus has become a global pandemic. 3CL protease is a virally encoded protein that is essential across a broad spectrum of coronaviruses with no close human analogs. PF-00835231, a 3CL protease inhibitor, has exhibited potent in vitro antiviral activity against SARS-CoV-2 as a single agent. Here we report, the design and characterization of a phosphate prodrug PF-07304814 to enable the delivery and projected sustained systemic exposure in human of PF-00835231 to inhibit coronavirus family 3CL protease activity with selectivity over human host protease targets. Furthermore, we show that PF-00835231 has additive/synergistic activity in combination with remdesivir. We present the ADME, safety, in vitro, and in vivo antiviral activity data that supports the clinical evaluation of PF-07304814 as a potential COVID-19 treatment.

Details

ISSN :
20411723
Volume :
12
Issue :
1
Database :
OpenAIRE
Journal :
Nature communications
Accession number :
edsair.doi.dedup.....a752e17863847bd64acf1c506536d2c9