Evidence map›Paper›PMID 33903855›Full record

ArticleEClinicalMedicine2021

Efficacy of the TMPRSS2 inhibitor camostat mesilate in patients hospitalized with Covid-19-a double-blind randomized controlled trial.

Jesper D Gunst, Nina B Staerke, Marie H Pahus, Lena H Kristensen, Jacob Bodilsen, Nicolai Lohse, Lars S Dalgaard, Dorthe Brønnum, Ole Fröbert, Bo Hønge and 29 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 NCT04321096 (The Impact of Camostat Mesilate on COVID-19 Infection), which is not on this map. Cited by 128 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed, 4 pooled it
11.6field-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.

NCT04321096 phase1 / phase2completednot on this map

The Impact of Camostat Mesilate on COVID-19 Infection: An Investigator-initiated Randomized, Placebo-controlled, Phase IIa Trial

TypeinterventionalSponsorUniversity of AarhusRan2020 to 2023Enrolled206ConditionsCorona Virus InfectionArmsCamostat Mesilate, Placebo oral tablet
3 · Its place in the literature

Who cites it

128 citing papers in PubMed, 4 syntheses or guidelines pooled it, 192 citations in OpenAlex.

  1. Pooled it
  2. COVID-19 pandemic: the delta variant, T-cell responses, and the efficacy of developing vaccines.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Pooled it
  3. Pooled it
  4. Pooled it
  5. One Week of Oral Camostat Versus Placebo in Nonhospitalized Adults With Mild-to-Moderate Coronavirus Disease 2019: A Randomized Controlled Phase 2 Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Trial
  6. 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
    Trial
  7. Trial
  8. Efficacy and safety of camostat mesylate in early COVID-19 disease in an ambulatory setting: a randomized placebo-controlled phase II trial.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Trial
  9. Trial
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  11. Review
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  13. Review
  14. Identification ofRSC medicinal chemistry · 2026
    Article
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68 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

39 authors at 10 institutions in 3 countries.

Jesper D GunstDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Nina B StaerkeDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Marie H PahusDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Lena H KristensenDepartment of Medicine, Viborg Regional Hospital, Denmark.
Jacob BodilsenDepartment of Infectious Diseases, Aalborg University Hospital, Denmark.
Nicolai LohseDepartment of Emergency Medicine, Copenhagen University Hospital, Hillerød, Denmark.
Lars S DalgaardDepartment of Medicine, Regional Hospital West Jutland, Herning, Denmark.
Dorthe BrønnumCentre for Clinical Research, North Denmark Regional Hospital, Hjoerring, Denmark.
Ole FröbertFaculty of Health, Dept. of Cardiology, Örebro University, Sweden.
Bo HøngeDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Isik S JohansenResearch Unit for Infectious Diseases, Odense University Hospital, University of Southern Denmark, Denmark.
Ida MonradDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Christian ErikstrupDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Regitze RosendalDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Emil VilstrupDepartment of Medicine, Viborg Regional Hospital, Denmark.
Theis MariagerDepartment of Infectious Diseases, Aalborg University Hospital, Denmark.
Dorthe G BoveDepartment of Emergency Medicine, Copenhagen University Hospital, Hillerød, Denmark.
Rasmus OffersenDepartment of Medicine, Regional Hospital West Jutland, Herning, Denmark.
Shakil ShakarDepartment of Internal Medicine, North Denmark Regional Hospital, Denmark.
Sara CajanderDepartment of Infectious Diseases, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Nis P JørgensenDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Sajitha S SritharanDepartment of Medicine, Viborg Regional Hospital, Denmark.
Peter BreiningDepartment of Clinical Pharmacology, Aarhus University Hospital, Aarhus, Denmark.
Søren JespersenDepartment of Emergency Medicine, Copenhagen University Hospital, Hillerød, Denmark.
Klaus L MortensenDepartment of Medicine, Regional Hospital West Jutland, Herning, Denmark.
Mads L JensenDepartment of Medicine, Viborg Regional Hospital, Denmark.
Lilian KolteDepartment of Lung and Infectious Diseases, Copenhagen University Hospital, Hillerød, Denmark.
Giacomo S FrattariDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Carsten S LarsenDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Merete StorgaardDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Lars P NielsenDepartment of Clinical Pharmacology, Aarhus University Hospital, Aarhus, Denmark.
Martin TolstrupDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Eva A SædderDepartment of Clinical Pharmacology, Aarhus University Hospital, Aarhus, Denmark.
Lars J ØstergaardDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Hien T T NgoDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Morten H JensenDepartment of Health Science and Technology, Aalborg University, Aalborg, Denmark.
Jesper F HøjenDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Mads KjolbyDepartment of Clinical Pharmacology, Aarhus University Hospital, Aarhus, Denmark.
Ole S SøgaardDepartment of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Aarhus University Hospital · DKAarhus University · DKCopenhagen University Hospital · DKRegional Hospital West Jutland · DKRegionshospitalet Viborg · DKSteno Diabetes Centers · DKAalborg University Hospital · DKNorth Denmark Region · DKÖrebro University · SEUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe trans-membrane protease serine 2 (TMPRSS2) is essential for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) cell entry and infection. Efficacy and safety of TMPRSS2 inhibitors in patients with coronavirus disease 2019 (Covid-19) have not been evaluated in randomized trials.

methodsWe conducted an investigator-initiated, double-blind, randomized, placebo-controlled multicenter trial in patients hospitalized with confirmed SARS-CoV-2 infection from April 4, to December 31, 2020. Within 48 h of admission, participants were randomly assigned in a 2:1 ratio to receive the TMPRSS2 inhibitor camostat mesilate 200 mg three times daily for 5 days or placebo. The primary outcome was time to discharge or clinical improvement measured as ≥2 points improvement on a 7-point ordinal scale. Other outcomes included 30-day mortality, safety and change in oropharyngeal viral load.

findings137 patients were assigned to receive camostat mesilate and 68 to placebo. Median time to clinical improvement was 5 days (interquartile range [IQR], 3 to 7) in the camostat group and 5 days (IQR, 2 to 10) in the placebo group (

interpretationUnder this protocol, camostat mesilate treatment was not associated with increased adverse events during hospitalization for Covid-19 and did not affect time to clinical improvement, progression to ICU admission or mortality. ClinicalTrials.gov Identifier: NCT04321096. EudraCT Number: 2020-001200-42.

Identifiers

PMID33903855
PMCPMC8060682
OpenAlexW3156990363

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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.