Evidence map›Paper›PMID 27736754›Full record

ArticleAntimicrobial agents and chemotherapy2017

Favipiravir Pharmacokinetics in Nonhuman Primates and Insights for Future Efficacy Studies of Hemorrhagic Fever Viruses.

Vincent Madelain, Jérémie Guedj, France Mentré, Thi Huyen Tram Nguyen, Frédéric Jacquot, Lisa Oestereich, Takumi Kadota, Koichi Yamada, Anne-Marie Taburet, Xavier de Lamballerie and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  14. Review
  15. Population pharmacokinetics of favipiravir in patients with COVID-19.CPT: pharmacometrics & systems pharmacology · 2021
    Observational
  16. Optimization of Analytical Procedure for In-hospital Rapid Quantification of Serum Level of Favipiravir in the Pharmacological Treatment of COVID-19.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2021
    Article
  17. Green micellar solvent-free HPLC and spectrofluorimetric determination of favipiravir as one of COVID-19 antiviral regimens.Microchemical journal : devoted to the application of microtechniques in all branches of science · 2021
    Article
  18. Article
  19. Influenza Therapeutics in Clinical Practice-Challenges and Recent Advances.Cold Spring Harbor perspectives in medicine · 2021
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Vincent MadelainIAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France vincent.madelain@inserm.fr.
Jérémie GuedjIAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
France MentréIAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Thi Huyen Tram NguyenIAME, UMR 1137, INSERM, Université Paris Diderot, Sorbonne Paris Cité, Paris, France.
Frédéric JacquotLaboratoire P4 INSERM-Jean Mérieux, US003 INSERM, Lyon, France.
Lisa OestereichBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Takumi KadotaDepartment of Research Laboratory of Toyama Chemical Co., Ltd., Tokyo, Japan.
Koichi YamadaDepartment of Research Laboratory of Toyama Chemical Co., Ltd., Tokyo, Japan.
Anne-Marie TaburetHopital Bicêtre, Assistance Publique-Hôpitaux de Paris, INSERM U1184, Center for Immunology of Viral Infections and Autoimmune Diseases, CEA, Université Paris-Sud, Kremlin Bicêtre, Paris, France.
Xavier de LamballerieUMR Emergence des Pathologies Virales (Aix-Marseille University-IRD 190-INSERM 1207-EHESP), Marseille, France.
Hervé RaoulLaboratoire P4 INSERM-Jean Mérieux, US003 INSERM, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Favipiravir is an RNA polymerase inhibitor that showed strong antiviral efficacy in vitro and in small-animal models of several viruses responsible for hemorrhagic fever (HF), including Ebola virus. The aim of this work was to characterize the complex pharmacokinetics of favipiravir in nonhuman primates (NHPs) in order to guide future efficacy studies of favipiravir in large-animal models. Four different studies were conducted in 30 uninfected cynomolgus macaques of Chinese (n = 17) or Mauritian (n = 13) origin treated with intravenous favipiravir for 7 to 14 days with maintenance doses of 60 to 180 mg/kg of body weight twice a day (BID). A pharmacokinetic model was developed to predict the plasma concentrations obtained with different dosing regimens, and the model predictions were compared to the 50% effective concentration (EC

Indexed as

Administration, IntravenousAldehyde OxidaseAmidesAnimalsAntiviral AgentsChlorocebus aethiopsEbolavirusHemorrhagic Fevers, ViralPrimatesPyrazinesVero CellsAldehyde OxidaseAmidesAntiviral AgentsfavipiravirPyrazinesfavipiravirhemorrhagic fevermodellingnonhuman primatespopulation pharmacokinetics

Identifiers

PMID27736754
PMCPMC5192134

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.