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Toward Consensus on Correct Interpretation of Protein Binding in Plasma and Other Biological Matrices for COVID-19 Therapeutic Development.
Boffito, Marta; Back, David J; Flexner, Charles; Sjö, Peter; Blaschke, Terrence F; Horby, Peter W; Cattaneo, Dario; Acosta, Edward P; Anderson, Peter; Owen, Andrew.
  • Boffito M; Chelsea & Westminster Hospital, London, UK.
  • Back DJ; Department of Infectious Disease, Imperial College London, London, UK.
  • Flexner C; Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
  • Sjö P; Bloomberg School of Public Health, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Blaschke TF; Drugs for Neglected Diseases Initiative (DNDi), Geneva, Switzerland.
  • Horby PW; Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Cattaneo D; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
  • Acosta EP; Unit of Clinical Pharmacology, ASST Fatebenefratelli, Sacco University Hospital, Milan, Italy.
  • Anderson P; Department of Pharmacology and Toxicology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Owen A; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Aurora, Colorado, USA.
Clin Pharmacol Ther ; 110(1): 64-68, 2021 07.
Article in English | MEDLINE | ID: covidwho-938406
ABSTRACT
The urgent global public health need presented by severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has brought scientists from diverse backgrounds together in an unprecedented international effort to rapidly identify interventions. There is a pressing need to apply clinical pharmacology principles and this has already been recognized by several other groups. However, one area that warrants additional specific consideration relates to plasma and tissue protein binding that broadly influences pharmacokinetics and pharmacodynamics. The principles of free drug theory have been forged and applied across drug development but are not currently being routinely applied for SARS-CoV-2 antiviral drugs. Consideration of protein binding is of critical importance to candidate selection but requires correct interpretation, in a drug-specific manner, to avoid either underinterpretation or overinterpretation of its consequences. This paper represents a consensus from international researchers seeking to apply historical knowledge, which has underpinned highly successful antiviral drug development for other viruses, such as HIV and hepatitis C virus for decades.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Drug Design / Drug Development / COVID-19 / COVID-19 Drug Treatment Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Clin Pharmacol Ther Year: 2021 Document Type: Article Affiliation country: Cpt.2099

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Drug Design / Drug Development / COVID-19 / COVID-19 Drug Treatment Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Clin Pharmacol Ther Year: 2021 Document Type: Article Affiliation country: Cpt.2099