An oral SARS-CoV-2 M <sup>pro</sup> inhibitor clinical candidate for the treatment of COVID-19

Dafydd R. Owen(Pfizer (United States)), Charlotte Allerton(Pfizer (United States)), Annaliesa S. Anderson(Pfizer (United States)), Lisa Aschenbrenner(Pfizer (United States)), Melissa Avery(Pfizer (United States)), Simon Berritt(Pfizer (United States)), Britton Boras(Pfizer (United States)), Rhonda D. Cardin(Pfizer (United States)), Anthony Carlo(Pfizer (United States)), Karen J. Coffman(Pfizer (United States)), Alyssa Dantonio(Pfizer (United States)), Li Di(Pfizer (United States)), Heather Eng(Pfizer (United States)), Rose Ann Ferre(Pfizer (United States)), K.S. Gajiwala(Pfizer (United States)), Scott Gibson(Utah State University), S.E. Greasley(Pfizer (United States)), Brett L. Hurst(Utah State University), Eugene P. Kadar(Pfizer (United States)), Amit S. Kalgutkar(Pfizer (United States)), Jack C. Lee(Pfizer (United States)), Jisun Lee(Pfizer (United States)), Wei Liu(Pfizer (United States)), Stephen W. Mason(Pfizer (United States)), Stephen Noell(Pfizer (United States)), Jonathan J. Novak(Pfizer (United States)), R. Scott Obach(Pfizer (United States)), Kevin Ogilvie(Pfizer (United States)), Nandini C. Patel(Pfizer (United States)), Martin Pettersson(Pfizer (United States)), Devendra K. Rai(Pfizer (United States)), Matthew R. Reese(Pfizer (United States)), M. F. Sammons(Pfizer (United States)), Jean G. Sathish(Pfizer (United States)), Ravi Shankar Prasad Singh(Pfizer (United States)), Claire M. Steppan(Pfizer (United States)), Al Stewart(Pfizer (United States)), Jamison B. Tuttle(Pfizer (United States)), Lawrence W. Updyke(Pfizer (United States)), Patrick R. Verhoest(Pfizer (United States)), Liuqing Wei(Pfizer (United States)), Qingyi Yang(Pfizer (United States)), Yuao Zhu(Pfizer (United States))
Science
November 2, 2021
Cited by 1,902Open Access
Full Text

Abstract

Path to another drug against COVID-19 The rapid development of vaccines has been crucial in battling the ongoing COVID-19 pandemic. However, access challenges remain, breakthrough infections occur, and emerging variants present increased risk. Developing antiviral therapeutics is therefore a high priority for the treatment of COVID-19. Some drug candidates in clinical trials act against the viral RNA-dependent RNA polymerase, but there are other viral enzymes that have been considered good targets for inhibition by drugs. Owen et al . report the discovery and characterization of a drug against the main protease involved in the cleavage of polyproteins involved in viral replication. The drug, PF-07321332, can be administered orally, has good selectivity and safety profiles, and protects against infection in a mouse model. In a phase 1 clinical trial, the drug reached concentrations expected to inhibit the virus based on in vitro studies. It also inhibited other coronaviruses, including severe acute respiratory syndrome coronavirus 1 and Middle East respiratory syndrome coronavirus, and could be in the armory against future viral threats. —VV


Related Papers

No related papers found

Powered by citation graph analysis