Evidence map›Paper›PMID 28769016›Full record

ReviewProceedings of the Japan Academy. Series B, Physical and biological sciences2017

Favipiravir (T-705), a broad spectrum inhibitor of viral RNA polymerase.

Yousuke Furuta, Takashi Komeno, Takaaki Nakamura

Open access · diamondAbstract readReview
In one paragraph

Review in Proceedings of the Japan Academy. Series B, Physical and biological sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 513 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
513citing papers in PubMed, 3 pooled it
63.1field-weighted citation impact, top 1% of its field
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

513 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,075 citations in OpenAlex.

  1. Pooled it
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  8. Multicenter, single-blind, randomized controlled study of the efficacy and safety of favipiravir and nafamostat mesilate in patients with COVID-19 pneumonia.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2023
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  11. Efficacy of favipiravir in adults with mild COVID-19: a randomized, double-blind, multicentre, placebo-controlled clinical trial.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2022
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453 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Yousuke FurutaBusiness Development Department, Toyama Chemical Co., Ltd.
Takashi KomenoPharmaceutical and Healthcare Research Laboratories, FUJIFILM Corporation.
Takaaki NakamuraResearch Laboratories, Toyama Chemical Co., Ltd.
Fujifilm (Japan) · JPLead Chemical (Japan) · JP

Funding

Vascular stabilization as a broad theraprutic platform for biodefenseU54AI065357 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI SCHWEIZER, HERBERT P. · 2005 to 2013
$77.5M
T CELL MEMORY TO VIRUSESR01AI030048 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI AHMED, RAFI · 1990 to 2022
$5.2M
T CELL MEMORY TO VIRUSESR37AI030048 · NIAID · EMORY UNIVERSITY · PI AHMED, RAFI · 2001 to 2010
$3.9M
ANIMAL MODELS OF HUMAN VIRAL INFECTIONS FOR EVALUATION OF EXPERIMENTAL-266015435N01AI015435 · NIAID · UTAH STATE UNIVERSITY · 2004 to 2004
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MACROPHAGE DEFENSES AGAINST HAEMOPHILUS INFLUENZAER29AI030063 · NIAID · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI NOEL, GARY J. · 1990 to 1994
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NIAID NIH HHS HHSN272201000039CNIAID NIH HHS HHSN272201000039INIAID NIH HHS HHSN272201100019CNIAID NIH HHS HHSN272201100019INIAID NIH HHS N01 AI015435NIAID NIH HHS N01 AI030048NIAID NIH HHS N01 AI030063NIAID NIH HHS U54 AI065357
6 · The paper itself

Abstract

Favipiravir (T-705; 6-fluoro-3-hydroxy-2-pyrazinecarboxamide) is an anti-viral agent that selectively and potently inhibits the RNA-dependent RNA polymerase (RdRp) of RNA viruses. Favipiravir was discovered through screening chemical library for anti-viral activity against the influenza virus by Toyama Chemical Co., Ltd. Favipiravir undergoes an intracellular phosphoribosylation to be an active form, favipiravir-RTP (favipiravir ribofuranosyl-5'-triphosphate), which is recognized as a substrate by RdRp, and inhibits the RNA polymerase activity. Since the catalytic domain of RdRp is conserved among various types of RNA viruses, this mechanism of action underpins a broader spectrum of anti-viral activities of favipiravir. Favipiravir is effective against a wide range of types and subtypes of influenza viruses, including strains resistant to existing anti-influenza drugs. Of note is that favipiravir shows anti-viral activities against other RNA viruses such as arenaviruses, bunyaviruses and filoviruses, all of which are known to cause fatal hemorrhagic fever. These unique anti-viral profiles will make favipiravir a potentially promising drug for specifically untreatable RNA viral infections.

Indexed as

AmidesAnimalsAntiviral AgentsDNA-Directed RNA PolymerasesEnzyme InhibitorsHumansPyrazinesVirusesAmidesAntiviral AgentsDNA-Directed RNA PolymerasesEnzyme InhibitorsfavipiravirPyrazinesbroad spectrum anti-viral agentfavipiravirinfluenza virusRNA-dependent RNA polymeraseRNA virusesviral hemorrhagic fever

Identifiers

PMID28769016
PMCPMC5713175
OpenAlexW2739679816

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.