Ivermectin for COVID-19 in adults in the community (PRINCIPLE): An open, randomised, controlled, adaptive platform trial of short- and longer-term outcomes

The evidence for whether ivermectin impacts recovery, hospital admissions, and longer-term outcomes in COVID-19 is contested. The WHO recommends its use only in the context of clinical trials. In this multicentre, open-label, multi-arm, adaptive platform randomised controlled trial, we included part...

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Veröffentlicht in:The Journal of infection 2024-04, Vol.88 (4), p.106130-106130, Article 106130
Hauptverfasser: Hayward, Gail, Yu, Ly-Mee, Little, Paul, Gbinigie, Oghenekome, Shanyinde, Milensu, Harris, Victoria, Dorward, Jienchi, Saville, Benjamin R., Berry, Nicholas, Evans, Philip H., Thomas, Nicholas P.B., Patel, Mahendra G., Richards, Duncan, Hecke, Oliver V., Detry, Michelle A., Saunders, Christina, Fitzgerald, Mark, Robinson, Jared, Latimer-Bell, Charlotte, Allen, Julie, Ogburn, Emma, Grabey, Jenna, de Lusignan, Simon, Hobbs, FD Richard, Butler, Christopher C.
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Sprache:eng
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Zusammenfassung:The evidence for whether ivermectin impacts recovery, hospital admissions, and longer-term outcomes in COVID-19 is contested. The WHO recommends its use only in the context of clinical trials. In this multicentre, open-label, multi-arm, adaptive platform randomised controlled trial, we included participants aged ≥18 years in the community, with a positive SARS-CoV-2 test, and symptoms lasting ≤14 days. Participants were randomised to usual care, usual care plus ivermectin tablets (target 300–400 μg/kg per dose, once daily for 3 days), or usual care plus other interventions. Co-primary endpoints were time to first self-reported recovery, and COVID-19 related hospitalisation/death within 28 days, analysed using Bayesian models. Recovery at 6 months was the primary, longer term outcome. Trial registration: ISRCTN86534580. The primary analysis included 8811 SARS-CoV-2 positive participants (median symptom duration 5 days), randomised to ivermectin (n = 2157), usual care (n = 3256), and other treatments (n = 3398) from June 23, 2021 to July 1, 2022. Time to self-reported recovery was shorter in the ivermectin group compared with usual care (hazard ratio 1·15 [95% Bayesian credible interval, 1·07 to 1·23], median decrease 2.06 days [1·00 to 3·06]), probability of meaningful effect (pre-specified hazard ratio ≥1.2) 0·192). COVID-19-related hospitalisations/deaths (odds ratio 1·02 [0·63 to 1·62]; estimated percentage difference 0% [−1% to 0·6%]), serious adverse events (three and five respectively), and the proportion feeling fully recovered were similar in both groups at 6 months (74·3% and 71·2% respectively (RR = 1·05, [1·02 to 1·08]) and also at 3 and 12 months. Ivermectin for COVID-19 is unlikely to provide clinically meaningful improvement in recovery, hospital admissions, or longer-term outcomes. Further trials of ivermectin for SARS-Cov-2 infection in vaccinated community populations appear unwarranted. UKRI/National Institute of Health Research (MC_PC_19079).
ISSN:0163-4453
1532-2742
DOI:10.1016/j.jinf.2024.106130