Analgesics
Antiandrogens
Antihistamines
Bromhexine
Budesonide
Colchicine
Conv. Plasma
Curcumin
Fluvoxamine
Hydroxychlor..
Ivermectin
Lifestyle
Melatonin
Metformin
Minerals
Monoclonals
Mpro inhibitors
Naso/orophar..
Nigella Sativa
Nitazoxanide
PPIs
Quercetin
RdRp inhibitors
Thermotherapy
Vitamins
More

Other
Feedback
Home
 
c19early.org COVID-19 treatment researchNafamostatNafamostat (more..)
Metformin Meta
Bromhexine Meta
Budesonide Meta
Colchicine Meta Nigella Sativa Meta
Conv. Plasma Meta Nitazoxanide Meta
Curcumin Meta PPIs Meta
Fluvoxamine Meta Quercetin Meta
Hydroxychlor.. Meta
Ivermectin Meta Thermotherapy Meta
Melatonin Meta

 
    
  
Nafamostat for COVID-19
7 studies from 177 scientists
16,265 patients in 4 countries
Significantly lower risk for viral clearance.
One study shows significant benefit.
COVID-19 Nafamostat studies. Apr 2025. c19early.org
0 0.5 1 1.5+ All studies 30% Mortality 4% Hospitalization -48% Recovery 29% Viral clearance 33% RCTs 35% RCT mortality 42% Early 33% Late 18% Favorsnafamostat Favorscontrol
Apr 28
Covid Analysis Nafamostat reduces COVID-19 risk: real-time meta analysis of 7 studies
Significantly lower risk is seen for viral clearance. One study shows significant benefit. Meta analysis using the most serious outcome reported shows 30% [10‑46%] lower risk. Results are similar for Randomized Controlled Trial..
Feb 14
2024
González-Paz et al., ACS Omega, doi:10.1021/acsomega.3c06968 Biophysical Analysis of Potential Inhibitors of SARS-CoV-2 Cell Recognition and Their Effect on Viral Dynamics in Different Cell Types: A Computational Prediction from In Vitro Experimental Data
In Silico study showing that nafamostat, camostat, chloroquine, hydroxychloroquine, telmisartan, and captopril may be beneficial for COVID-19 by inhibiting SARS-CoV-2 cell entry and replication in multiple cell types expressing ACE2 and T..
Oct 24
2023
Morpeth et al., NEJM Evidence, doi:10.1056/EVIDoa2300132 A Randomized Trial of Nafamostat for Covid-19
55% lower ventilation (p=0.23), 57% lower progression (p=0.14), and 28% improved recovery (p=0.36). RCT 160 hospitalized non-critically ill COVID-19 patients showing a 93% posterior probability that nafamostat reduced the odds of death or receipt of ventilatory or vasopressor support by day 28 compared to usual care. Nafamostat, a TMPRS..
Oct 19
2023
Seccia et al., Journal of Clinical Medicine, doi:10.3390/jcm12206618 RAndomized Clinical Trial Of NAfamostat Mesylate, A Potent Transmembrane Protease Serine 2 (TMPRSS2) Inhibitor, in Patients with COVID-19 Pneumonia
67% lower mortality (p=1) and 20% improved recovery (p=1). RCT 15 hospitalized COVID-19 patients showing a positive safety profile with nafamostat mesylate treatment. While the study was underpowered to detect differences in efficacy, Bayesian analysis suggested a signal for potential benefit (69..
Sep 30
2023
Okugawa et al., International Journal of Antimicrobial Agents, doi:10.1016/j.ijantimicag.2023.106922 Antiviral effect and safety of nafamostat mesilate in patients with mild early-onset COVID-19: An exploratory multicentre randomized controlled clinical trial
33% improved viral clearance (p=0.007). RCT 30 early-onset COVID-19 patients showing significantly improved viral load reduction with nafamostat.
Feb 8
2023
Seydi et al., NCT04390594 Multicentre, Open Label, Randomised, Adaptative Clinical Trial of Efficacy and Safety of Treatment Regimens in Adult COVID-19 Patients in Senegal
59 patient nafamostat late treatment RCT with results not reported over 2 years after completion.
Sep 30
2022
Soma et al., Japanese Journal of Infectious Diseases, doi:10.7883/yoken.JJID.2021.699 Nafamostat Mesylate Monotherapy in Patients with Moderate COVID-19: a Single-Center, Retrospective Study
80% lower mortality (p=0.49) and 6% higher severe cases (p=1). Retrospective 64 hospitalized patients with moderate COVID-19 showing no significant difference in clinical outcomes with nafamostat mesylate.
Aug 1
2022
Kim et al., NCT04871646 A Double-blind, Multi-center, Multi-regional, Randomized Controlled, Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of CKD-314 in Hospitalized Adult Patients Diagnosed With COVID-19
Estimated 586 patient nafamostat late treatment RCT with results not reported over 2 years after estimated completion.
Jun 30
2022
Umar et al., Jurnal Teknologi Laboratorium, doi:10.29238/teknolabjournal.v11i1.344 Inhibitory potentials of ivermectin, nafamostat, and camostat on spike protein and some nonstructural proteins of SARS-CoV-2: Virtual screening approach
In Silico study of ivermectin, camostat, and nafamostat, showing that ivermectin had the best inhibitory action on the SARS-CoV-2 spike protein and Nsp10, while nafamostat had the best results for the other non-structural proteins. Author..
Feb 28
2022
Quinn et al., eBioMedicine, doi:10.1016/j.ebiom.2022.103856 Randomised controlled trial of intravenous nafamostat mesylate in COVID pneumonitis: Phase 1b/2a experimental study to investigate safety, Pharmacokinetics and Pharmacodynamics
48% longer hospitalization (p=0.21). RCT 42 hospitalized patients with COVID-19 pneumonitis showing no benefit with intravenous nafamostat mesylate.
Feb 7
2022
Schultz et al., Nature, doi:10.1038/s41586-022-04482-x Pyrimidine inhibitors synergize with nucleoside analogues to block SARS-CoV-2
In Vitro and mouse study showing synergistic antiviral effects when combining pyrimidine biosynthesis inhibitors with antiviral nucleoside analogues against SARS-CoV-2. Authors screened 18 thousand drugs and validated 122 with antiviral a..
Dec 31
2021
Hempel et al., Chemical Science, doi:10.1039/D1SC01494C Synergistic inhibition of SARS-CoV-2 cell entry by otamixaban and covalent protease inhibitors: pre-clinical assessment of pharmacological and molecular properties
In Vitro study showing that otamixaban inhibits SARS-CoV-2 cell entry through TMPRSS2 inhibition. Authors found otamixaban to be a weak TMPRSS2 inhibitor in cell culture (IC50 of 18.7 μM) compared to camostat (IC50 of 151.1 nM) and nafamo..
Dec 26
2021
Inokuchi et al., Journal of Clinical Medicine, doi:10.3390/jcm11010116 Association between Nafamostat Mesylate and In-Hospital Mortality in Patients with Coronavirus Disease 2019: A Multicenter Observational Study
27% higher mortality (p=0.52). Retrospective multicenter observational study of 15,859 hospitalized COVID-19 patients in Japan showing no significant difference in in-hospital mortality with nafamostat mesylate. Very few patients received treatment and they had more se..
Nov 30
2021
Zhuravel et al., eClinicalMedicine, doi:10.1016/j.eclinm.2021.101169 Nafamostat in hospitalized patients with moderate to severe COVID-19 pneumonia: a randomised Phase II clinical trial
76% lower mortality (p=0.2), 42% greater improvement (p=0.28), and 42% improved recovery (p=0.28). RCT 104 hospitalized patients with moderate to severe COVID-19 pneumonia showing no significant difference in the primary endpoint of time to clinical improvement with nafamostat. However, in patients with baseline National Early Warning ..
Apr 30
2021
Sgrignani et al., Frontiers in Molecular Biosciences, doi:10.3389/fmolb.2021.666626 Computational Identification of a Putative Allosteric Binding Pocket in TMPRSS2
In Silico study of TMPRSS2 inhibition by camostat, nafamostat, and bromhexine, suggesting allosteric binding for bromhexine, compared to camostat and nafamostat which bind to the active site of TMPRSS2 forming covalent adducts.
Apr 30
2021
Bae et al., NCT04418128 Treatment Effect of Nafamostat Mesylate in Patients With COVID-19 Pneumonia: Open Labelled Randomized Controlled Clinical Trial
Estimated 84 patient nafamostat late treatment RCT with results not reported over 4 years after estimated completion.
Apr 5
2021
Kim et al., NCT04628143 Open-label, Multi-center, Randomized Controlled, Phase 2 Clinical Trial to Evaluate the Efficacy and Safety of CKD-314 in Hospitalized Adult Patients Diagnosed With COVID-19
13 patient nafamostat late treatment RCT with results not reported over 4 years after completion.
Please send us corrections, updates, or comments. c19early involves the extraction of 100,000+ datapoints from thousands of papers. Community updates help ensure high accuracy. Treatments and other interventions are complementary. All practical, effective, and safe means should be used based on risk/benefit analysis. No treatment or intervention is 100% available and effective for all current and future variants. We do not provide medical advice. Before taking any medication, consult a qualified physician who can provide personalized advice and details of risks and benefits based on your medical history and situation. IMA and WCH provide treatment protocols.
  or use drag and drop   
Thanks for your feedback! Please search before submitting papers and note that studies are listed under the date they were first available, which may be the date of an earlier preprint.
Submit