Rationale of a loading dose initiation for hydroxychloroquine treatment in COVID-19 infection in the DisCoVeRy trial.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 09 2020
Historique:
pubmed: 31 5 2020
medline: 4 9 2020
entrez: 31 5 2020
Statut: ppublish

Résumé

Around the world, several dose regimens of hydroxychloroquine have been used for COVID-19 infection treatment, with the objective of identifying a short-term course. Hydroxychloroquine was found to decrease the viral replication in a concentration-dependent manner in vitro and to be more active when added prior to the viral challenge. A loading dose is used to rapidly attain a target drug concentration, which is usually considered as approximately the steady-state concentration. With a loading dose, the minimum effective concentration is reached much more rapidly than when using only the maintenance dose from the start. Thus, we propose a hydroxychloroquine sulphate dose regimen of 400 mg twice daily at Day 1 then 400 mg once daily from Day 2 to Day 10. We aim to evaluate this in the C-20-15 DisCoVeRy trial.

Identifiants

pubmed: 32473020
pii: 5849074
doi: 10.1093/jac/dkaa191
pmc: PMC7314033
doi:

Substances chimiques

Hydroxychloroquine 4QWG6N8QKH

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2376-2380

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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Auteurs

Minh Patrick Lê (MP)

AP-HP, Bichat Claude Bernard Hospital, Pharmacology-Toxicology Department, 75018 Paris, France.
INSERM, UMRS-1144, Université de Paris, 75006 Paris, France.

Nathan Peiffer-Smadja (N)

AP-HP, Bichat Claude Bernard Hospital, Tropical and infectious diseases Department, 75018 Paris, France.
IAME, INSERM, UMRS1137, Université de Paris, 75018 Paris, France.

Jeremie Guedj (J)

IAME, INSERM, UMRS1137, Université de Paris, 75018 Paris, France.

Nadège Néant (N)

IAME, INSERM, UMRS1137, Université de Paris, 75018 Paris, France.

France Mentré (F)

IAME, INSERM, UMRS1137, Université de Paris, 75018 Paris, France.

Florence Ader (F)

Hospices Civils de Lyon, Department of Infectious Diseases, Croix-Rousse Hospital, 104 Grande-Rue de la Croix-Rousse, Lyon 69004, France.
Université Claude Bernard Lyon 1, Inserm, 1111, Centre International de Recherche en Infectiologie (CIRI) UCBL1, Lyon, France.

Yazdan Yazdanpanah (Y)

AP-HP, Bichat Claude Bernard Hospital, Tropical and infectious diseases Department, 75018 Paris, France.
IAME, INSERM, UMRS1137, Université de Paris, 75018 Paris, France.

Gilles Peytavin (G)

AP-HP, Bichat Claude Bernard Hospital, Pharmacology-Toxicology Department, 75018 Paris, France.
IAME, INSERM, UMRS1137, Université de Paris, 75018 Paris, France.

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Classifications MeSH