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Remdesivir: Quo vadis?
De Clercq, Erik.
  • De Clercq E; KU Leuven, Department of Microbiology, Immunology & Transplantation, Rega Institute for Medical Research, Herestraat 49, 3000 Leuven, Belgium. Electronic address: erik.declercq@kuleuven.be.
Biochem Pharmacol ; 193: 114800, 2021 11.
Article in English | MEDLINE | ID: covidwho-1471892
ABSTRACT
Remdesivir (GS-5734, Veklury®) has remained the only antiviral drug formally approved by the US FDA for the treatment of Covid-19 (SARS-CoV-2 infection). Its key structural features are the fact that it is a C-nucleoside (adenosine) analogue, contains a 1'-cyano function, and could be considered as a ProTide based on the presence of a phosphoramidate group. Its antiviral spectrum and activity in animal models have been well established and so has been its molecular mode of action as a delayed chain terminator of the viral RdRp (RNA-dependent RNA polymerase). Its clinical efficacy has been evaluated, but needs to be optimized with regard to timing, dosage and duration of treatment, and route of administration. Safety, toxicity and pharmacokinetics need to be further addressed, and so are its potential combinations with other drugs such as corticosteroids (i.e. dexamethasone) and ribavirin.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Adenosine Monophosphate / Alanine / SARS-CoV-2 / COVID-19 Drug Treatment Type of study: Experimental Studies / Prognostic study Limits: Animals / Humans Language: English Journal: Biochem Pharmacol Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Adenosine Monophosphate / Alanine / SARS-CoV-2 / COVID-19 Drug Treatment Type of study: Experimental Studies / Prognostic study Limits: Animals / Humans Language: English Journal: Biochem Pharmacol Year: 2021 Document Type: Article