Evidence map›Paper›PMID 36823196›Full record

ArticleScientific reports2023

Expanded profiling of Remdesivir as a broad-spectrum antiviral and low potential for interaction with other medications in vitro.

Sheli R Radoshitzky, Patrick Iversen, Xianghan Lu, Jing Zou, Suzanne J F Kaptein, Kelly S Stuthman, Sean A Van Tongeren, Jesse Steffens, Ruoyu Gong, Hoa Truong and 19 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
17.7field-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

40 citing papers in PubMed, 61 citations in OpenAlex.

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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

29 authors at 9 institutions in 2 countries.

Sheli R RadoshitzkyThe Geneva Foundation, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD, USA.
Patrick IversenThe Geneva Foundation, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD, USA.
Xianghan LuGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Jing ZouDepartment of Biochemistry & Molecular Biology, Institute for Drug Discovery, Sealy Center for Structural Biology & Molecular Biophysics, University of Texas Medical Branch, Galveston, TX, USA.
Suzanne J F KapteinKU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute for Medical Research, B-3000, Leuven, Belgium.
Kelly S StuthmanThe Geneva Foundation, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD, USA.
Sean A Van TongerenThe Geneva Foundation, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD, USA.
Jesse SteffensThe Geneva Foundation, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD, USA.
Ruoyu GongGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Hoa TruongGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Annapurna A SapreGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Huiling YangGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Xiaodong XieGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Jia Jun ChiaGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Zhijuan J SongGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Stacey M LeventhalGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Josolyn ChanGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Alex ShornikovGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Xin ZhangKU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute for Medical Research, B-3000, Leuven, Belgium.
David CowferGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Helen YuGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Travis WarrenThe Geneva Foundation, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD, USA.
Tomas CihlarGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Danielle P PorterGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Johan NeytsKU Leuven Department of Microbiology, Immunology and Transplantation, Laboratory of Virology and Chemotherapy, Rega Institute for Medical Research, B-3000, Leuven, Belgium.
Pei-Yong ShiDepartment of Biochemistry & Molecular Biology, Institute for Drug Discovery, Sealy Center for Structural Biology & Molecular Biophysics, University of Texas Medical Branch, Galveston, TX, USA.
Jay WellsThe Geneva Foundation, United States Army Medical Research Institute of Infectious Diseases (USAMRIID), Fort Detrick, Frederick, MD, USA.
John P BilelloGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA.
Joy Y FengGilead Sciences, Inc, 333 Lakeside Drive, Foster City, CA, USA. joy.feng@gilead.com.
Gilead Sciences (United States) · USUnited States Army · USThe University of Texas Medical Branch at Galveston · USUnited States Army Medical Research Institute of Infectious Diseases · USCenter for Drug Evaluation and Research · USGlobal Virus Network · USKU Leuven · BERega Institute for Medical Research · BEThe Geneva Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Remdesivir (GS-5734; VEKLURY) is a single diastereomer monophosphoramidate prodrug of an adenosine analog (GS-441524). Remdesivir is taken up by target cells and metabolized in multiple steps to form the active nucleoside triphosphate (GS-443902), which acts as a potent inhibitor of viral RNA-dependent RNA polymerases. Remdesivir and GS-441524 have antiviral activity against multiple RNA viruses. Here, we expand the evaluation of remdesivir's antiviral activity to members of the families Flaviviridae, Picornaviridae, Filoviridae, Orthomyxoviridae, and Hepadnaviridae. Using cell-based assays, we show that remdesivir can inhibit infection of flaviviruses (such as dengue 1-4, West Nile, yellow fever, Zika viruses), picornaviruses (such as enterovirus and rhinovirus), and filoviruses (such as various Ebola, Marburg, and Sudan virus isolates, including novel geographic isolates), but is ineffective or is significantly less effective against orthomyxoviruses (influenza A and B viruses), or hepadnaviruses B, D, and E. In addition, remdesivir shows no antagonistic effect when combined with favipiravir, another broadly acting antiviral nucleoside analog, and has minimal interaction with a panel of concomitant medications. Our data further support remdesivir as a broad-spectrum antiviral agent that has the potential to address multiple unmet medical needs, including those related to antiviral pandemic preparedness.

Indexed as

FiloviridaeHemorrhagic Fever, EbolaZika VirusZika Virus InfectionAdenosine MonophosphateAlanineAntiviral AgentsHumansAdenosine MonophosphateAlanineAntiviral Agentsremdesivir

Identifiers

PMID36823196
PMCPMC9950143
OpenAlexW4321596571

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.