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The oral protease inhibitor (PF-07321332) protects Syrian hamsters against infection with SARS-CoV-2 variants of concern.

Rana AbdelnabiShi-Yan Caroline FooDirk JochmansLaura VangeelSteven De JonghePatrick AugustijnsRaf MolsBirgit WeynandThanaporn WattanakulRichard M HoglundJoel TarningCharles E MowbrayPeter SjöFanny EscudieIvan ScandaleEric ChatelainJohan Neyts
Published in: Nature communications (2022)
There is an urgent need for potent and selective antivirals against SARS-CoV-2. Pfizer developed PF-07321332 (PF-332), a potent inhibitor of the viral main protease (Mpro, 3CLpro) that can be dosed orally and that is in clinical development. We here report that PF-332 exerts equipotent in vitro activity against the four SARS-CoV-2 variants of concerns (VoC) and that it can completely arrest replication of the alpha variant in primary human airway epithelial cells grown at the air-liquid interface. Treatment of Syrian Golden hamsters with PF-332 (250 mg/kg, twice daily) completely protected the animals against intranasal infection with the beta (B.1.351) and delta (B.1.617.2) SARS-CoV-2 variants. Moreover, treatment of SARS-CoV-2 (B.1.617.2) infected animals with PF-332 completely prevented transmission to untreated co-housed sentinels.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • copy number
  • endothelial cells
  • cell proliferation
  • combination therapy
  • replacement therapy
  • pluripotent stem cells