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521. A phase II, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate COVID-19 disease

BACKGROUND: Tafenoquine is an 8-aminoquinoline antimalarial approved by the US FDA for malaria prevention and is being evaluated in clinical trials for potential use in other disease areas. METHODS: The safety and efficacy of tafenoquine administered as a 200 mg dose once per day on days 1, 2, 3, an...

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Autor principal: Dow, Geoffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678769/
http://dx.doi.org/10.1093/ofid/ofad500.590
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author Dow, Geoffrey
author_facet Dow, Geoffrey
author_sort Dow, Geoffrey
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description BACKGROUND: Tafenoquine is an 8-aminoquinoline antimalarial approved by the US FDA for malaria prevention and is being evaluated in clinical trials for potential use in other disease areas. METHODS: The safety and efficacy of tafenoquine administered as a 200 mg dose once per day on days 1, 2, 3, and 10 was evaluated over a 28-day period in mild-moderate COVID-19 patients. The primary endpoint was Day 14 clinical recovery from COVID-19 symptoms, defined as cough mild or absent, respiratory rate < 24 bpm, and no shortness of breath or fever. Following a successful futility analysis after n = 86 patients out of a target n = 275 were randomized, the study was terminated and unblinded early to facilitate planning for confirmatory studies. RESULTS: The proportion of patients not recovered on Day 14 was numerically decreased by 27% in the ITT population [8/45 v 10/42 not recovered in the tafenoquine and placebo arms, P = 0.60] and 47% in the PP population [5/42 v 9/41, P = 0.25]. Amongst individuals who recorded responses in an electronic diary at Day 28, all tafenoquine patients were recovered, whereas up to 12% of placebo patients exhibited lingering dyspnea. Time to clinical recovery from COVID-19 symptoms was accelerated in the tafenoquine arm by about 2-2.5 days. There were two COVID-19 related hospitalizations in the placebo arm and one in the tafenoquine arm. Mild, drug related adverse events occurred in 8.4% of individuals in the tafenoquine arm [v 2.4% in the placebo]. CONCLUSION: Although this trial was underpowered for the primary endpoint due to its early termination, the data are suggestive of a therapeutic benefit associated with tafenoquine administration in outpatients with mild to moderate COVID-19 disease, and larger studies are planned. DISCLOSURES: Geoffrey Dow, PhD, 60 Degrees Pharmaceuticals, INC: Board Member|60 Degrees Pharmaceuticals, INC: Inventor on Company covid + malaria patents|60 Degrees Pharmaceuticals, INC: Ownership Interest
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spelling pubmed-106787692023-11-27 521. A phase II, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate COVID-19 disease Dow, Geoffrey Open Forum Infect Dis Abstract BACKGROUND: Tafenoquine is an 8-aminoquinoline antimalarial approved by the US FDA for malaria prevention and is being evaluated in clinical trials for potential use in other disease areas. METHODS: The safety and efficacy of tafenoquine administered as a 200 mg dose once per day on days 1, 2, 3, and 10 was evaluated over a 28-day period in mild-moderate COVID-19 patients. The primary endpoint was Day 14 clinical recovery from COVID-19 symptoms, defined as cough mild or absent, respiratory rate < 24 bpm, and no shortness of breath or fever. Following a successful futility analysis after n = 86 patients out of a target n = 275 were randomized, the study was terminated and unblinded early to facilitate planning for confirmatory studies. RESULTS: The proportion of patients not recovered on Day 14 was numerically decreased by 27% in the ITT population [8/45 v 10/42 not recovered in the tafenoquine and placebo arms, P = 0.60] and 47% in the PP population [5/42 v 9/41, P = 0.25]. Amongst individuals who recorded responses in an electronic diary at Day 28, all tafenoquine patients were recovered, whereas up to 12% of placebo patients exhibited lingering dyspnea. Time to clinical recovery from COVID-19 symptoms was accelerated in the tafenoquine arm by about 2-2.5 days. There were two COVID-19 related hospitalizations in the placebo arm and one in the tafenoquine arm. Mild, drug related adverse events occurred in 8.4% of individuals in the tafenoquine arm [v 2.4% in the placebo]. CONCLUSION: Although this trial was underpowered for the primary endpoint due to its early termination, the data are suggestive of a therapeutic benefit associated with tafenoquine administration in outpatients with mild to moderate COVID-19 disease, and larger studies are planned. DISCLOSURES: Geoffrey Dow, PhD, 60 Degrees Pharmaceuticals, INC: Board Member|60 Degrees Pharmaceuticals, INC: Inventor on Company covid + malaria patents|60 Degrees Pharmaceuticals, INC: Ownership Interest Oxford University Press 2023-11-27 /pmc/articles/PMC10678769/ http://dx.doi.org/10.1093/ofid/ofad500.590 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Dow, Geoffrey
521. A phase II, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate COVID-19 disease
title 521. A phase II, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate COVID-19 disease
title_full 521. A phase II, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate COVID-19 disease
title_fullStr 521. A phase II, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate COVID-19 disease
title_full_unstemmed 521. A phase II, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate COVID-19 disease
title_short 521. A phase II, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate COVID-19 disease
title_sort 521. a phase ii, double blind, placebo-controlled, randomized evaluation of the safety and efficacy of tafenoquine in patients with mild-moderate covid-19 disease
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678769/
http://dx.doi.org/10.1093/ofid/ofad500.590
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