Use of ivermectin in the treatment of Covid-19: A pilot trial
Objectives: In this randomized open-label trial pilot study we assessed the antiviral effects and safety of various doses of ivermectin in patients with mild clinical symptoms of COVID-19. Methods: Patients were randomly assigned to receive standard of care (SOC) treatment at hospital admission; SOC...
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2021-01-01
|
Series: | Toxicology Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2214750021000445 |
id |
doaj-faef5ce491224ec6b8cc5e373fbb0c99 |
---|---|
record_format |
Article |
spelling |
doaj-faef5ce491224ec6b8cc5e373fbb0c992021-03-13T04:22:54ZengElsevierToxicology Reports2214-75002021-01-018505510Use of ivermectin in the treatment of Covid-19: A pilot trialHenrique Pott-Junior0Mônica Maria Bastos Paoliello1Alice de Queiroz Constantino Miguel2Anderson Ferreira da Cunha3Caio Cesar de Melo Freire4Fábio Fernandes Neves5Lucimar Retto da Silva de Avó6Meliza Goi Roscani7Sigrid De Sousa dos Santos8Silvana Gama Florêncio Chachá9Department of Medicine, Federal University of São Carlos (UFSCar), 13565-905, São Carlos, São Paulo, Brazil; Corresponding author at: Department of Medicine, Federal University of São Carlos, Rod. Washington Luis, km 235, São Carlos, SP, Brazil.Department of Molecular Pharmacology, Albert Einstein College of Medicine, 10461, Bronx, New York, United StatesUniversity Hospital of the Federal University of São Carlos (UFSCar), 13565-905, São Carlos, São Paulo, BrazilDepartment of Genetics and Evolution, Federal University of São Carlos (UFSCar); 13565-905, São Carlos, São Paulo, BrazilDepartment of Genetics and Evolution, Federal University of São Carlos (UFSCar); 13565-905, São Carlos, São Paulo, BrazilDepartment of Medicine, Federal University of São Carlos (UFSCar), 13565-905, São Carlos, São Paulo, BrazilDepartment of Medicine, Federal University of São Carlos (UFSCar), 13565-905, São Carlos, São Paulo, BrazilDepartment of Medicine, Federal University of São Carlos (UFSCar), 13565-905, São Carlos, São Paulo, BrazilDepartment of Medicine, Federal University of São Carlos (UFSCar), 13565-905, São Carlos, São Paulo, BrazilDepartment of Medicine, Federal University of São Carlos (UFSCar), 13565-905, São Carlos, São Paulo, BrazilObjectives: In this randomized open-label trial pilot study we assessed the antiviral effects and safety of various doses of ivermectin in patients with mild clinical symptoms of COVID-19. Methods: Patients were randomly assigned to receive standard of care (SOC) treatment at hospital admission; SOC plus ivermectin 100 mcg/kg; SOC plus ivermectin 200 mcg/kg; or SOC plus ivermectin 400 mcg/kg. The primary assessed endpoint was the proportion of patients who achieved two consecutive negative SARS-CoV-2 RT PCR tests within 7 days of the start of the dosing period. This study was registered at ClinicalTrials.gov (NCT04431466). Results: A total of 32 patients were enrolled and randomized to treatment. SOC treatment together with ivermectin did not result in any serious adverse events. All patients exhibited a reduction in SARS-CoV-2 viral load within 7 days; however, those who received ivermectin had a more consistent decrease as compared to the SOC alone group, characterized by a shorter time for obtaining two consecutive negative SARS-CoV-2 RT PCR tests. Conclusions: Ivermectin is safe in patients with SARS-CoV-2, reducing symptomatology and the SARS-CoV-2 viral load. This antiviral effect appears to depend on the dose used, and if confirmed in future studies, it suggests that ivermectin may be a useful adjuvant to the SOC treatment in patients with mild COVID-19 symptoms.http://www.sciencedirect.com/science/article/pii/S2214750021000445IvermectinCOVID-19SARS-CoV-2 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Henrique Pott-Junior Mônica Maria Bastos Paoliello Alice de Queiroz Constantino Miguel Anderson Ferreira da Cunha Caio Cesar de Melo Freire Fábio Fernandes Neves Lucimar Retto da Silva de Avó Meliza Goi Roscani Sigrid De Sousa dos Santos Silvana Gama Florêncio Chachá |
spellingShingle |
Henrique Pott-Junior Mônica Maria Bastos Paoliello Alice de Queiroz Constantino Miguel Anderson Ferreira da Cunha Caio Cesar de Melo Freire Fábio Fernandes Neves Lucimar Retto da Silva de Avó Meliza Goi Roscani Sigrid De Sousa dos Santos Silvana Gama Florêncio Chachá Use of ivermectin in the treatment of Covid-19: A pilot trial Toxicology Reports Ivermectin COVID-19 SARS-CoV-2 |
author_facet |
Henrique Pott-Junior Mônica Maria Bastos Paoliello Alice de Queiroz Constantino Miguel Anderson Ferreira da Cunha Caio Cesar de Melo Freire Fábio Fernandes Neves Lucimar Retto da Silva de Avó Meliza Goi Roscani Sigrid De Sousa dos Santos Silvana Gama Florêncio Chachá |
author_sort |
Henrique Pott-Junior |
title |
Use of ivermectin in the treatment of Covid-19: A pilot trial |
title_short |
Use of ivermectin in the treatment of Covid-19: A pilot trial |
title_full |
Use of ivermectin in the treatment of Covid-19: A pilot trial |
title_fullStr |
Use of ivermectin in the treatment of Covid-19: A pilot trial |
title_full_unstemmed |
Use of ivermectin in the treatment of Covid-19: A pilot trial |
title_sort |
use of ivermectin in the treatment of covid-19: a pilot trial |
publisher |
Elsevier |
series |
Toxicology Reports |
issn |
2214-7500 |
publishDate |
2021-01-01 |
description |
Objectives: In this randomized open-label trial pilot study we assessed the antiviral effects and safety of various doses of ivermectin in patients with mild clinical symptoms of COVID-19. Methods: Patients were randomly assigned to receive standard of care (SOC) treatment at hospital admission; SOC plus ivermectin 100 mcg/kg; SOC plus ivermectin 200 mcg/kg; or SOC plus ivermectin 400 mcg/kg. The primary assessed endpoint was the proportion of patients who achieved two consecutive negative SARS-CoV-2 RT PCR tests within 7 days of the start of the dosing period. This study was registered at ClinicalTrials.gov (NCT04431466). Results: A total of 32 patients were enrolled and randomized to treatment. SOC treatment together with ivermectin did not result in any serious adverse events. All patients exhibited a reduction in SARS-CoV-2 viral load within 7 days; however, those who received ivermectin had a more consistent decrease as compared to the SOC alone group, characterized by a shorter time for obtaining two consecutive negative SARS-CoV-2 RT PCR tests. Conclusions: Ivermectin is safe in patients with SARS-CoV-2, reducing symptomatology and the SARS-CoV-2 viral load. This antiviral effect appears to depend on the dose used, and if confirmed in future studies, it suggests that ivermectin may be a useful adjuvant to the SOC treatment in patients with mild COVID-19 symptoms. |
topic |
Ivermectin COVID-19 SARS-CoV-2 |
url |
http://www.sciencedirect.com/science/article/pii/S2214750021000445 |
work_keys_str_mv |
AT henriquepottjunior useofivermectininthetreatmentofcovid19apilottrial AT monicamariabastospaoliello useofivermectininthetreatmentofcovid19apilottrial AT alicedequeirozconstantinomiguel useofivermectininthetreatmentofcovid19apilottrial AT andersonferreiradacunha useofivermectininthetreatmentofcovid19apilottrial AT caiocesardemelofreire useofivermectininthetreatmentofcovid19apilottrial AT fabiofernandesneves useofivermectininthetreatmentofcovid19apilottrial AT lucimarrettodasilvadeavo useofivermectininthetreatmentofcovid19apilottrial AT melizagoiroscani useofivermectininthetreatmentofcovid19apilottrial AT sigriddesousadossantos useofivermectininthetreatmentofcovid19apilottrial AT silvanagamaflorenciochacha useofivermectininthetreatmentofcovid19apilottrial |
_version_ |
1724222243682123776 |