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AGILE: a seamless phase I/IIa platform for the rapid evaluation of candidates for COVID-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter

BACKGROUND: There is an urgent unmet clinical need for the identification of novel therapeutics for the treatment of COVID-19. A number of COVID-19 late phase trial platforms have been developed to investigate (often repurposed) drugs both in the UK and globally (e.g. RECOVERY led by the University...

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Autores principales: Griffiths, Gareth O., FitzGerald, Richard, Jaki, Thomas, Corkhill, Andrea, Reynolds, Helen, Ewings, Sean, Condie, Susannah, Tilt, Emma, Johnson, Lucy, Radford, Mike, Simpson, Catherine, Saunders, Geoffrey, Yeats, Sara, Mozgunov, Pavel, Tansley-Hancock, Olana, Martin, Karen, Downs, Nichola, Eberhart, Izabela, Martin, Jonathan W. B., Goncalves, Cristiana, Song, Anna, Fletcher, Tom, Byrne, Kelly, Lalloo, David G., Owen, Andrew, Jacobs, Michael, Walker, Lauren, Lyon, Rebecca, Woods, Christie, Gibney, Jennifer, Chiong, Justin, Chandiwana, Nomathemba, Jacob, Shevin, Lamorde, Mohammed, Orrell, Catherine, Pirmohamed, Munir, Khoo, Saye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311065/
https://www.ncbi.nlm.nih.gov/pubmed/34311777
http://dx.doi.org/10.1186/s13063-021-05458-4
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author Griffiths, Gareth O.
FitzGerald, Richard
Jaki, Thomas
Corkhill, Andrea
Reynolds, Helen
Ewings, Sean
Condie, Susannah
Tilt, Emma
Johnson, Lucy
Radford, Mike
Simpson, Catherine
Saunders, Geoffrey
Yeats, Sara
Mozgunov, Pavel
Tansley-Hancock, Olana
Martin, Karen
Downs, Nichola
Eberhart, Izabela
Martin, Jonathan W. B.
Goncalves, Cristiana
Song, Anna
Fletcher, Tom
Byrne, Kelly
Lalloo, David G.
Owen, Andrew
Jacobs, Michael
Walker, Lauren
Lyon, Rebecca
Woods, Christie
Gibney, Jennifer
Chiong, Justin
Chandiwana, Nomathemba
Jacob, Shevin
Lamorde, Mohammed
Orrell, Catherine
Pirmohamed, Munir
Khoo, Saye
author_facet Griffiths, Gareth O.
FitzGerald, Richard
Jaki, Thomas
Corkhill, Andrea
Reynolds, Helen
Ewings, Sean
Condie, Susannah
Tilt, Emma
Johnson, Lucy
Radford, Mike
Simpson, Catherine
Saunders, Geoffrey
Yeats, Sara
Mozgunov, Pavel
Tansley-Hancock, Olana
Martin, Karen
Downs, Nichola
Eberhart, Izabela
Martin, Jonathan W. B.
Goncalves, Cristiana
Song, Anna
Fletcher, Tom
Byrne, Kelly
Lalloo, David G.
Owen, Andrew
Jacobs, Michael
Walker, Lauren
Lyon, Rebecca
Woods, Christie
Gibney, Jennifer
Chiong, Justin
Chandiwana, Nomathemba
Jacob, Shevin
Lamorde, Mohammed
Orrell, Catherine
Pirmohamed, Munir
Khoo, Saye
author_sort Griffiths, Gareth O.
collection PubMed
description BACKGROUND: There is an urgent unmet clinical need for the identification of novel therapeutics for the treatment of COVID-19. A number of COVID-19 late phase trial platforms have been developed to investigate (often repurposed) drugs both in the UK and globally (e.g. RECOVERY led by the University of Oxford and SOLIDARITY led by WHO). There is a pressing need to investigate novel candidates within early phase trial platforms, from which promising candidates can feed into established later phase platforms. AGILE grew from a UK-wide collaboration to undertake early stage clinical evaluation of candidates for SARS-CoV-2 infection to accelerate national and global healthcare interventions. METHODS/DESIGN: AGILE is a seamless phase I/IIa platform study to establish the optimum dose, determine the activity and safety of each candidate and recommend whether it should be evaluated further. Each candidate is evaluated in its own trial, either as an open label single arm healthy volunteer study or in patients, randomising between candidate and control usually in a 2:1 allocation in favour of the candidate. Each dose is assessed sequentially for safety usually in cohorts of 6 patients. Once a phase II dose has been identified, efficacy is assessed by seamlessly expanding into a larger cohort. AGILE is completely flexible in that the core design in the master protocol can be adapted for each candidate based on prior knowledge of the candidate (i.e. population, primary endpoint and sample size can be amended). This information is detailed in each candidate specific trial protocol of the master protocol. DISCUSSION: Few approved treatments for COVID-19 are available such as dexamethasone, remdesivir and tocilizumab in hospitalised patients. The AGILE platform aims to rapidly identify new efficacious and safe treatments to help end the current global COVID-19 pandemic. We currently have three candidate specific trials within this platform study that are open to recruitment. TRIAL REGISTRATION: EudraCT Number: 2020-001860-27 14 March 2020 ClinicalTrials.gov Identifier: NCT04746183 19 February 2021 ISRCTN reference: 27106947 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-021-05458-4.
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spelling pubmed-83110652021-07-26 AGILE: a seamless phase I/IIa platform for the rapid evaluation of candidates for COVID-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter Griffiths, Gareth O. FitzGerald, Richard Jaki, Thomas Corkhill, Andrea Reynolds, Helen Ewings, Sean Condie, Susannah Tilt, Emma Johnson, Lucy Radford, Mike Simpson, Catherine Saunders, Geoffrey Yeats, Sara Mozgunov, Pavel Tansley-Hancock, Olana Martin, Karen Downs, Nichola Eberhart, Izabela Martin, Jonathan W. B. Goncalves, Cristiana Song, Anna Fletcher, Tom Byrne, Kelly Lalloo, David G. Owen, Andrew Jacobs, Michael Walker, Lauren Lyon, Rebecca Woods, Christie Gibney, Jennifer Chiong, Justin Chandiwana, Nomathemba Jacob, Shevin Lamorde, Mohammed Orrell, Catherine Pirmohamed, Munir Khoo, Saye Trials Update BACKGROUND: There is an urgent unmet clinical need for the identification of novel therapeutics for the treatment of COVID-19. A number of COVID-19 late phase trial platforms have been developed to investigate (often repurposed) drugs both in the UK and globally (e.g. RECOVERY led by the University of Oxford and SOLIDARITY led by WHO). There is a pressing need to investigate novel candidates within early phase trial platforms, from which promising candidates can feed into established later phase platforms. AGILE grew from a UK-wide collaboration to undertake early stage clinical evaluation of candidates for SARS-CoV-2 infection to accelerate national and global healthcare interventions. METHODS/DESIGN: AGILE is a seamless phase I/IIa platform study to establish the optimum dose, determine the activity and safety of each candidate and recommend whether it should be evaluated further. Each candidate is evaluated in its own trial, either as an open label single arm healthy volunteer study or in patients, randomising between candidate and control usually in a 2:1 allocation in favour of the candidate. Each dose is assessed sequentially for safety usually in cohorts of 6 patients. Once a phase II dose has been identified, efficacy is assessed by seamlessly expanding into a larger cohort. AGILE is completely flexible in that the core design in the master protocol can be adapted for each candidate based on prior knowledge of the candidate (i.e. population, primary endpoint and sample size can be amended). This information is detailed in each candidate specific trial protocol of the master protocol. DISCUSSION: Few approved treatments for COVID-19 are available such as dexamethasone, remdesivir and tocilizumab in hospitalised patients. The AGILE platform aims to rapidly identify new efficacious and safe treatments to help end the current global COVID-19 pandemic. We currently have three candidate specific trials within this platform study that are open to recruitment. TRIAL REGISTRATION: EudraCT Number: 2020-001860-27 14 March 2020 ClinicalTrials.gov Identifier: NCT04746183 19 February 2021 ISRCTN reference: 27106947 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13063-021-05458-4. BioMed Central 2021-07-26 /pmc/articles/PMC8311065/ /pubmed/34311777 http://dx.doi.org/10.1186/s13063-021-05458-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Update
Griffiths, Gareth O.
FitzGerald, Richard
Jaki, Thomas
Corkhill, Andrea
Reynolds, Helen
Ewings, Sean
Condie, Susannah
Tilt, Emma
Johnson, Lucy
Radford, Mike
Simpson, Catherine
Saunders, Geoffrey
Yeats, Sara
Mozgunov, Pavel
Tansley-Hancock, Olana
Martin, Karen
Downs, Nichola
Eberhart, Izabela
Martin, Jonathan W. B.
Goncalves, Cristiana
Song, Anna
Fletcher, Tom
Byrne, Kelly
Lalloo, David G.
Owen, Andrew
Jacobs, Michael
Walker, Lauren
Lyon, Rebecca
Woods, Christie
Gibney, Jennifer
Chiong, Justin
Chandiwana, Nomathemba
Jacob, Shevin
Lamorde, Mohammed
Orrell, Catherine
Pirmohamed, Munir
Khoo, Saye
AGILE: a seamless phase I/IIa platform for the rapid evaluation of candidates for COVID-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter
title AGILE: a seamless phase I/IIa platform for the rapid evaluation of candidates for COVID-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter
title_full AGILE: a seamless phase I/IIa platform for the rapid evaluation of candidates for COVID-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter
title_fullStr AGILE: a seamless phase I/IIa platform for the rapid evaluation of candidates for COVID-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter
title_full_unstemmed AGILE: a seamless phase I/IIa platform for the rapid evaluation of candidates for COVID-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter
title_short AGILE: a seamless phase I/IIa platform for the rapid evaluation of candidates for COVID-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter
title_sort agile: a seamless phase i/iia platform for the rapid evaluation of candidates for covid-19 treatment: an update to the structured summary of a study protocol for a randomised platform trial letter
topic Update
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311065/
https://www.ncbi.nlm.nih.gov/pubmed/34311777
http://dx.doi.org/10.1186/s13063-021-05458-4
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