Author: Jorgensen, Sarah CJ; Kebriaei, Razieh; Dresser, Linda D
Title: Remdesivir: Review of pharmacology, preâ€clinical data and emerging clinical experience for COVIDâ€19 Cord-id: uo8k6qic Document date: 2020_5_23
ID: uo8k6qic
Snippet: The global pandemic of novel coronavirus disease 2019 (COVIDâ€19) caused by severe acute respiratory syndrome coronavirus 2 (SARSâ€CoVâ€2) has created an urgent need for effective antivirals. Remdesivir (formerly GSâ€5734) is a nucleoside analogue proâ€drug currently being evaluated in COVIDâ€19 clinical trials. Its unique structural features allow high concentrations of the active triphosphate metabolite to be delivered intracellularly and it evades proofreading to successfully inhibit vi
Document: The global pandemic of novel coronavirus disease 2019 (COVIDâ€19) caused by severe acute respiratory syndrome coronavirus 2 (SARSâ€CoVâ€2) has created an urgent need for effective antivirals. Remdesivir (formerly GSâ€5734) is a nucleoside analogue proâ€drug currently being evaluated in COVIDâ€19 clinical trials. Its unique structural features allow high concentrations of the active triphosphate metabolite to be delivered intracellularly and it evades proofreading to successfully inhibit viral RNA synthesis. In preâ€clinical models, remdesivir has demonstrated potent antiviral activity against diverse human and zoonotic βâ€coronaviruses, including SARSâ€CoVâ€2. In this article we critically review available data on remdesivir with an emphasis on biochemistry, pharmacology, pharmacokinetics and in vitro activity against coronaviruses as well as clinical experience and current progress in COVIDâ€19 clinical trials.
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