Evidence map›Paper›PMID 37018987›Full record

ReviewBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie2023

Paxlovid (Nirmatrelvir/Ritonavir): A new approach to Covid-19 therapy?

Seyed Mohammad Reza Hashemian, Amirhossein Sheida, Mohammad Taghizadieh, Mohammad Yousef Memar, Michael R Hamblin, Hossein Bannazadeh Baghi, Javid Sadri Nahand, Zatollah Asemi, Hamed Mirzaei

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
30.5field-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

78 citing papers in PubMed, 157 citations in OpenAlex.

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18 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

9 authors at 4 institutions in 2 countries.

Seyed Mohammad Reza HashemianCritical Care Department, National Research Institute ofTuberculosis and Lung Disease, Shahid Beheshti University of Medical Science,Tehran, Iran; Chronic Respiratory Disease Research Center, National ResearchInstitute of Tuberculosis and Lung Disease, Shahid Beheshti University ofMedical Science, Tehran, Iran.
Amirhossein SheidaSchool of Medicine, Kashan University of Medical Sciences, Kashan, Iran; Student Research Committee, Kashan Universityof Medical Sciences, Kashan, Iran.
Mohammad TaghizadiehDepartment of Pathology, School of Medicine, Center for Women'sHealth Research Zahra, Tabriz University of Medical Sciences, Tabriz, Iran.
Mohammad Yousef MemarInfectious and Tropical Diseases Research Center, Tabriz Universityof Medical Sciences, Tabriz, Iran.
Michael R HamblinLaser Research Centre, Faculty of Health Science, University of Johannesburg, Doornfontein 2028, South Africa.
Hossein Bannazadeh BaghiInfectious and Tropical Diseases Research Center, Tabriz Universityof Medical Sciences, Tabriz, Iran.
Javid Sadri NahandInfectious and Tropical Diseases Research Center, Tabriz Universityof Medical Sciences, Tabriz, Iran. Electronic address: javidsadri65@gmail.com.
Zatollah AsemiResearch Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran.
Hamed MirzaeiResearch Center for Biochemistry and Nutrition in Metabolic Diseases, Institute for Basic Sciences, Kashan University of Medical Sciences, Kashan, Iran. Electronic address: mirzaei-h@kaums.ac.ir.
Tabriz University of Medical Sciences · IRKashan University of Medical Sciences · IRShahid Beheshti University · IRUniversity of Johannesburg · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the need for novel, effective therapeutics for the COVID-19 pandemic, no curative regimen is yet available, therefore patients are forced to rely on supportive and nonspecific therapies. Some SARS-CoV-2 proteins, like the 3 C-like protease (3CLpro) or the major protease (Mpro), have been identified as promising targets for antiviral drugs. The Mpro has major a role in protein processing as well as pathogenesis of the virus, and could be a useful therapeutic target. The antiviral drug nirmatrelvir can keep SARS-CoV-2 from replicating through inhibiting Mpro. Nirmatrelvir was combined with another HIV protease inhibitor, ritonavir, to create Paxlovid (Nirmatrelvir/Ritonavir). The metabolizing enzyme cytochrome P450 3 A is inhibited by ritonavir to lengthen the half-life of nirmatrelvir, so rintonavir acts as a pharmacological enhancer. Nirmatrelvir exhibits potent antiviral activity against current coronavirus variants, despite significant alterations in the SARS-CoV-2 viral genome. Nevertheless, there are still several unanswered questions. This review summarizes the current literature on nirmatrelvir and ritonavir efficacy in treating SARS-CoV-2 infection, and also their safety and possible side effects.

Indexed as

COVID-19HIV Protease InhibitorsAntiviral AgentsCOVID-19 Drug TreatmentDrug CombinationsHumansLactamsLeucineNitrilesPandemicsPeptide HydrolasesProlineRitonavirSARS-CoV-2Antiviral AgentsDrug CombinationsHIV Protease InhibitorsLactamsLeucinenirmatrelvir and ritonavir drug combinationNitrilesPeptide HydrolasesProlineRitonavir3 C-like proteaseCOVID-19NirmatrelvirPaxlovidRitonavirSARS-CoV-2

Identifiers

PMID37018987
PMCPMC9899776
OpenAlexW4319319486

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.