Evidence map›Paper›PMID 34222849›Full record

ArticleEClinicalMedicine2021

Effect of Tenofovir Disoproxil Fumarate and Emtricitabine on nasopharyngeal SARS-CoV-2 viral load burden amongst outpatients with COVID-19: A pilot, randomized, open-label phase 2 trial.

Jean-Jacques Parienti, Thierry Prazuck, Laure Peyro-Saint-Paul, Anna Fournier, Cécile Valentin, Sylvie Brucato, Renaud Verdon, Aymeric Sève, Mathilda Colin, Fabien Lesne and 5 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in EClinicalMedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04685512 (Effect of Tenofovir/Emtricitabine Short Course on Viral Clearance in Patients Recently Infected With SARS-COV2), which is not on this map. Cited by 43 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 5 pooled it
4.0field-weighted citation impact, top 5% 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.

NCT04685512 phase2 / phase3completednot on this map

Effect of Tenofovir/Emtricitabine Short Course on Viral Clearance in Patients Recently Infected With SARS-COV2 (Covid-19) Not Requiring Hospitalization: a Phase IIB/III Multicenter Open-label Randomized Controlled Trial

TypeinterventionalSponsorUniversity Hospital, CaenRan2020 to 2021Enrolled60ConditionsCovid19Armstenofovir disoproxil and emtricitabine
3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 5 syntheses or guidelines pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Antiviral drug treatment for nonsevere COVID-19: a systematic review and network meta-analysis.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2022
    Pooled it
  6. Daily tenofovir disoproxil fumarate/emtricitabine and hydroxychloroquine for pre-exposure prophylaxis of COVID-19: a double-blind placebo-controlled randomized trial in healthcare workers.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2023
    Trial
  7. Review
  8. Article
  9. Promising Drugs Require Proper Testing.Clinical and translational science · 2026
    Article
  10. Review
  11. Article
  12. Review
  13. Plausible mechanism of drug resistance and side-effects of COVID-19 therapeutics: a bottleneck for its eradication.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2024
    Review
  14. COVID-19 therapeutics.Clinical microbiology reviews · 2024
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article
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

15 authors at 2 institutions in 1 country.

Jean-Jacques ParientiDepartment of Clinical Research and Innovation, Caen University Hospital, Caen, France.
Thierry PrazuckDepartment of Infectious Diseases, Orléans Regional Hospital, Orléans, France.
Laure Peyro-Saint-PaulDepartment of Clinical Research and Innovation, Caen University Hospital, Caen, France.
Anna FournierDepartment of Infectious Diseases, Caen University Hospital, Caen, France.
Cécile ValentinDepartment of Clinical Research and Innovation, Caen University Hospital, Caen, France.
Sylvie BrucatoDepartment of Clinical Research and Innovation, Caen University Hospital, Caen, France.
Renaud VerdonDepartment of Infectious Diseases, Caen University Hospital, Caen, France.
Aymeric SèveDepartment of Infectious Diseases, Orléans Regional Hospital, Orléans, France.
Mathilda ColinDepartment of Infectious Diseases, Orléans Regional Hospital, Orléans, France.
Fabien LesneDepartment of Virology, Orléans Regional Hospital, Orléans, France.
Jérome GuinardDepartment of Virology, Orléans Regional Hospital, Orléans, France.
Meriadeg Ar GouilhEA 2656 - Groupe de recherche sur l'adaptation microbienne 2.0, UNICAEN-Université de Caen Normandie, Caen, France.
Julia DinaEA 2656 - Groupe de recherche sur l'adaptation microbienne 2.0, UNICAEN-Université de Caen Normandie, Caen, France.
Astrid VabretEA 2656 - Groupe de recherche sur l'adaptation microbienne 2.0, UNICAEN-Université de Caen Normandie, Caen, France.
Laurent HocquelouxDepartment of Infectious Diseases, Orléans Regional Hospital, Orléans, France.
Université de Caen Normandie · FRCentre hospitalier universitaire d'Orléans · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTenofovir and emtricitabine interfere with the SARS CoV-2 ribonucleic acid (RNA)-dependent RNA polymerase (RdRp). Several cohorts reported that people treated by tenofovir disoproxil fumarate and emtricitabine are less likely to develop SARS CoV-2 infection and related severe COVID-19.

methodsWe conducted a pilot randomized, open-label, controlled, phase 2 trial at two hospitals in France. Eligible patients were consecutive outpatients (aged ≥18 years) with RT-PCR-confirmed SARS-CoV-2 infection and an interval from symptom onset to enrolment of 7 days or less. Patients were randomly assigned in a 1:1 ratio to receive oral tenofovir disoproxil fumarate and emtricitabine (2 pills on day 1 followed by 1 pill per day on days 2-7) or the standard of care. The primary and secondary endpoints were SARS-CoV-2 viral clearance from baseline assessed by cycle threshold (Ct) RT-PCR on nasopharyngeal swab collected at day 4 and day 7, respectively. A higher Ct corresponds to a lower SARS CoV-2 viral burden. Other endpoints were the time to recovery and the number of adverse events. This trial is registered with ClinicalTrials.gov, NCT04685512.

findingsFrom November, 20

interpretationIn this pilot study of outpatients adult with recent non-severe COVID-19, tenofovir disoproxil fumarate plus emtricitabine appeared to accelerate the natural clearance of nasopharyngeal SARS-CoV-2 viral burden. These findings support the conduct of larger trials of tenofovir-based therapies for the prevention and early treatment of COVID-19.

fundingNo external funding.

Identifiers

PMID34222849
PMCPMC8235994
OpenAlexW3176158657

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.