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Pharmacometrics of high-dose ivermectin in early COVID-19 from an open label, randomized, controlled adaptive platform trial (PLATCOV)

Authors :
William HK Schilling
Podjanee Jittamala
James A Watson
Maneerat Ekkapongpisit
Tanaya Siripoon
Thundon Ngamprasertchai
Viravarn Luvira
Sasithorn Pongwilai
Cintia Cruz
James J Callery
Simon Boyd
Varaporn Kruabkontho
Thatsanun Ngernseng
Jaruwan Tubprasert
Mohammad Yazid Abdad
Nattaporn Piaraksa
Kanokon Suwannasin
Pongtorn Hanboonkunupakarn
Borimas Hanboonkunupakarn
Sakol Sookprome
Kittiyod Poovorawan
Janjira Thaipadungpanit
Stuart Blacksell
Mallika Imwong
Joel Tarning
Walter RJ Taylor
Vasin Chotivanich
Chunlanee Sangketchon
Wiroj Ruksakul
Kesinee Chotivanich
Mauro Martins Teixeira
Sasithon Pukrittayakamee
Arjen M Dondorp
Nicholas PJ Day
Watcharapong Piyaphanee
Weerapong Phumratanaprapin
Nicholas J White
on behalf of the PLATCOV Collaborative Group
Source :
eLife, Vol 12 (2023)
Publication Year :
2023
Publisher :
eLife Sciences Publications Ltd, 2023.

Abstract

Background: There is no generally accepted methodology for in vivo assessment of antiviral activity in SARS-CoV-2 infections. Ivermectin has been recommended widely as a treatment of COVID-19, but whether it has clinically significant antiviral activity in vivo is uncertain. Methods: In a multicentre open label, randomized, controlled adaptive platform trial, adult patients with early symptomatic COVID-19 were randomized to one of six treatment arms including high-dose oral ivermectin (600 µg/kg daily for 7 days), the monoclonal antibodies casirivimab and imdevimab (600 mg/600 mg), and no study drug. The primary outcome was the comparison of viral clearance rates in the modified intention-to-treat population. This was derived from daily log10 viral densities in standardized duplicate oropharyngeal swab eluates. This ongoing trial is registered at https://clinicaltrials.gov/ (NCT05041907). Results: Randomization to the ivermectin arm was stopped after enrolling 205 patients into all arms, as the prespecified futility threshold was reached. Following ivermectin, the mean estimated rate of SARS-CoV-2 viral clearance was 9.1% slower (95% confidence interval [CI] –27.2% to +11.8%; n=45) than in the no drug arm (n=41), whereas in a preliminary analysis of the casirivimab/imdevimab arm it was 52.3% faster (95% CI +7.0% to +115.1%; n=10 (Delta variant) vs. n=41). Conclusions: High-dose ivermectin did not have measurable antiviral activity in early symptomatic COVID-19. Pharmacometric evaluation of viral clearance rate from frequent serial oropharyngeal qPCR viral density estimates is a highly efficient and well-tolerated method of assessing SARS-CoV-2 antiviral therapeutics in vivo. Funding: ‘Finding treatments for COVID-19: A phase 2 multi-centre adaptive platform trial to assess antiviral pharmacodynamics in early symptomatic COVID-19 (PLAT-COV)’ is supported by the Wellcome Trust Grant ref: 223195/Z/21/Z through the COVID-19 Therapeutics Accelerator. Clinical trial number: NCT05041907.

Details

Language :
English
ISSN :
2050084X
Volume :
12
Database :
Directory of Open Access Journals
Journal :
eLife
Publication Type :
Academic Journal
Accession number :
edsdoj.2c1da5e8a0a4bd4bce22cc5135ee7e1
Document Type :
article
Full Text :
https://doi.org/10.7554/eLife.83201