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Get Free AccessBackground: Ensitrelvir is an oral antiviral treatment for COVID-19 with the same molecular target as ritonavir-boosted nirmatrelvir - the current oral first-line treatment. There have been no direct comparisons between the two drugs. Methods: In an open label controlled adaptive pharmacometric platform trial, low-risk adult patients aged 18-60 years with early symptomatic COVID-19 (<4 days of symptoms) were randomised concurrently to one of eight treatment arms including ensitrelvir, ritonavir-boosted nirmatrelvir, and no study drug. The primary endpoint was the rate of oropharyngeal viral clearance assessed in a modified intention-to-treat population (mITT), defined as patients with >3 days of follow-up. Viral clearance rate was derived under a Bayesian hierarchical linear model fitted to the log10 viral densities in standardised duplicate oropharyngeal swab eluates taken daily over five days (14 measurements). This trial is registered at ClinicalTrials.gov ( NCT05041907 ). Findings: Between March 2023 and April 2024 the three study arms randomised 604 patients concurrently in Thailand and Lao PDR (ensitrelvir 202; ritonavir-boosted nirmatrelvir 207; no study drug 195) among 903 patients enrolled. All patients recovered uneventfully. Ensitrelvir was very well tolerated and did not cause dysgeusia. Median (interquartile range) estimated SARS-CoV-2 clearance half-lives were 5.9 hours (4.0 to 8.6) with ensitrelvir; 5.2 hours (3.8 to 6.6) with nirmatrelvir; and 11.6 hours (8.1 to 14.5) with no study drug. Viral clearance following ensitrelvir was 82% (95% credible interval, CrI: 61 to 104%) faster than no study drug and 16% (95% CrI: 5 to 25%) slower than ritonavir-boosted nirmatrelvir. Viral rebound occurred in 15 (7%) of the nirmatrelvir group and 10 (5%) of the ensitrelvir group (p=0.4). Conclusions: Both ensitrelvir and nirmatrelvir markedly accelerate oropharyngeal SARS-CoV-2 viral clearance. Ensitrelvir is an efficacious and well tolerated alternative to currently available antivirals in treating COVID-19. 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.
William HK Schilling, Podjanee Jittamala, Phrutsamon Wongnak, James A Watson, Simon Boyd, Viravarn Luvira, Tanaya Siripoon, Thundon Ngamprasertchai, Elizabeth M. Batty, Ellen M. Beer, Shivani Singh, Tanatchakorn Asawasriworanan, Timothy Seers, Koukeo Phommasone, Terry John Evans, Varaporn Kruabkontho, Thatsanun Ngernseng, Jaruwan Tubprasert, Mohammad Yazid Abdad, Wanassanan Madmanee, Jindarat Kouhathong, Kanokon Suwannasin, Watcharee Pagornrat, Tianrat Piteekan, Borimas Hanboonkunupakarn, Kittiyod Poovorawan, Manus Potaporn, Attasit Srisubat, Bootsakorn Loharjun, Kesinee Chotivanich, Mallika Imwong, Sasithon Pukrittayakamee, Arjen M. Dondorp, Nicholas Day, Watcharapong Piyaphanee, Weerapong Phumratanaprapin, Sir Nicholas White (2025). Antiviral efficacy of oral ensitrelvir versus oral ritonavir-boosted nirmatrelvir in COVID-19. , DOI: https://doi.org/10.1101/2025.05.18.25327861.
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Type
Preprint
Year
2025
Authors
37
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1101/2025.05.18.25327861
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