Abstract
The worldwide outbreak of COVID-19 caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become a global pandemic. Alongside vaccines, antiviral therapeutics are an important part of the healthcare response to countering the ongoing threat presented by COVID-19. Here, we report the discovery and characterization of PF-07321332, an orally bioavailable SARS-CoV-2 main protease inhibitor with in vitro pan-human coronavirus antiviral activity and excellent off-target selectivity and in vivo safety profiles. PF-07321332 has demonstrated oral activity in a mouse-adapted SARS-CoV-2 model and has achieved oral plasma concentrations exceeding the in vitro antiviral cell potency in a phase 1 clinical trial in healthy human participants.
MeSH terms
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Administration, Oral
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Animals
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COVID-19 / virology
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COVID-19 Drug Treatment*
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Clinical Trials, Phase I as Topic
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Coronavirus / drug effects
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Disease Models, Animal
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Drug Therapy, Combination
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Humans
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Lactams / administration & dosage
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Lactams / pharmacokinetics
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Lactams / pharmacology*
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Lactams / therapeutic use*
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Leucine / administration & dosage
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Leucine / pharmacokinetics
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Leucine / pharmacology*
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Leucine / therapeutic use*
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Mice
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Mice, Inbred BALB C
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Microbial Sensitivity Tests
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Nitriles / administration & dosage
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Nitriles / pharmacokinetics
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Nitriles / pharmacology*
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Nitriles / therapeutic use*
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Proline / administration & dosage
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Proline / pharmacokinetics
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Proline / pharmacology*
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Proline / therapeutic use*
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Randomized Controlled Trials as Topic
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Ritonavir / administration & dosage
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Ritonavir / therapeutic use
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SARS-CoV-2 / drug effects*
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SARS-CoV-2 / physiology
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Viral Protease Inhibitors / administration & dosage
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Viral Protease Inhibitors / pharmacokinetics
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Viral Protease Inhibitors / pharmacology*
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Viral Protease Inhibitors / therapeutic use*
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Virus Replication / drug effects
Substances
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Lactams
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Nitriles
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Viral Protease Inhibitors
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nirmatrelvir
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Proline
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Leucine
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Ritonavir
Associated data
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figshare/10.25454/ pfizer.figshare.16699669