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

Britton BorasRhys M JonesBrandon J AnsonDan ArensonLisa AschenbrennerMalina A BakowskiNathan BeutlerJoseph BinderEmily ChenHeather EngHolly HammondJennifer HammondRobert E HauptRobert L HoffmanEugene P KadarRob KaniaEmi KimotoMelanie G KirkpatrickLorraine LanyonEmma K LendyJonathan R LillisJames P LogueSuman A LuthraChunlong MaStephen W MasonMarisa E McGrathStephen NoellR Scott ObachMatthew N O' BrienRebecca O'ConnorKevin OgilvieDafydd OwenMartin PetterssonMatthew R ReeseThomas F RogersRomel RosalesMichelle I RossulekJean G SathishNorimitsu ShiraiClaire SteppanMartyn TicehurstLawrence W UpdykeStuart M WestonYuao ZhuKris M WhiteAdolfo García-SastreJun WangArnab K ChatterjeeAndrew D MesecarMatthew B FriemannAnnaliesa S AndersonCharlotte Allerton
Published in: Nature communications (2021)
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.
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