Removal of Remdesivir’s Metabolite GS-441524 by Hemodialysis in a Double Lung Transplant Recipient with COVID-19

Author:

Lê Minh Patrick12ORCID,Le Hingrat Quentin34ORCID,Jaquet Pierre5,Wicky Paul-Henri5,Bunel Vincent6,Massias Laurent14,Visseaux Benoit34ORCID,Messika Jonathan6,Descamps Diane34,Mal Hervé6,Timsit Jean-François45,Peytavin Gilles14ORCID

Affiliation:

1. AP-HP, Bichat Claude Bernard Hospital, Pharmacology-Toxicology Department, Paris, France

2. INSERM, UMRS 1144, Université de Paris, Paris, France

3. AP-HP, Bichat Claude Bernard Hospital, Virology Department, Paris, France

4. IAME, INSERM, UMRS 1137, Université de Paris, Paris, France

5. AP-HP, Bichat Claude Bernard Hospital, Medical and Infectious Diseases ICU (MI2), Paris, France

6. AP-HP, Bichat Claude Bernard Hospital, Pneumology B and Lung Transplant Department, INSERM 1152, Paris, France

Abstract

Remdesivir has reported efficacy against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in vitro and in vivo . Drug-drug interactions limit therapeutic options in transplant patients. Remdesivir and its metabolite GS-441524 are excreted principally in urine. In intensive care unit (ICU) settings, in which multiple-organ dysfunctions can occur rapidly, hemodialysis may be a viable option for maintaining remdesivir treatment, while improving tolerance, by removing both remdesivir’s metabolite (GS-441524) and sulfobutylether β-cyclodextrin sodium (SEBCD).

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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