Back to Search Start Over

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

Authors :
Boras B
Jones RM
Anson BJ
Arenson D
Aschenbrenner L
Bakowski MA
Beutler N
Binder J
Chen E
Eng H
Hammond H
Hammond J
Haupt RE
Hoffman R
Kadar EP
Kania R
Kimoto E
Kirkpatrick MG
Lanyon L
Lendy EK
Lillis JR
Logue J
Luthra SA
Ma C
Mason SW
McGrath ME
Noell S
Obach RS
O' Brien MN
O'Connor R
Ogilvie K
Owen D
Pettersson M
Reese MR
Rogers TF
Rosales R
Rossulek MI
Sathish JG
Shirai N
Steppan C
Ticehurst M
Updyke LW
Weston S
Zhu Y
White KM
García-Sastre A
Wang J
Chatterjee AK
Mesecar AD
Frieman MB
Anderson AS
Allerton C
Source :
Nature communications [Nat Commun] 2021 Oct 18; Vol. 12 (1), pp. 6055. Date of Electronic Publication: 2021 Oct 18.
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.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
34663813
Full Text :
https://doi.org/10.1038/s41467-021-26239-2