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The impact of rarity in NICE’s health technology appraisals

BACKGROUND: In the absence of a framework designed to evaluate medicines for rare diseases in the UK, most orphan medicines are appraised by the National Institute for Health and Care Excellence (NICE) through the Single Technology Appraisal (STA) process. RESULTS: An analysis of STA appraisals of o...

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Autores principales: Clarke, Sophie, Ellis, Michelle, Brownrigg, Jack
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117316/
https://www.ncbi.nlm.nih.gov/pubmed/33985575
http://dx.doi.org/10.1186/s13023-021-01845-x
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author Clarke, Sophie
Ellis, Michelle
Brownrigg, Jack
author_facet Clarke, Sophie
Ellis, Michelle
Brownrigg, Jack
author_sort Clarke, Sophie
collection PubMed
description BACKGROUND: In the absence of a framework designed to evaluate medicines for rare diseases in the UK, most orphan medicines are appraised by the National Institute for Health and Care Excellence (NICE) through the Single Technology Appraisal (STA) process. RESULTS: An analysis of STA appraisals of orphan and non-orphan medicines revealed that orphan medicines were subject to a significantly longer mean time in the NICE process than non-orphan medicines [370 days (n = 44) vs. 277 days (n = 118), p =  < 0.0001]. A higher proportion of orphan STAs required more than one Appraisal Committee Meeting (ACM) versus non-orphan STAs, and orphan STAs were disadvantaged by worse outcomes with respect to positive recommendations than those orphan medicines assessed by Highly Specialised Technology evaluation (HST). CONCLUSIONS: The uncertainties inherent to developing orphan medicines may contribute to these disadvantages. Improved understanding of the challenges in drug development for orphan medicines and clearer guidance for decision makers on navigating uncertainty in the HTA process may promote greater equity in access to medicines across rare and common conditions.
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spelling pubmed-81173162021-05-13 The impact of rarity in NICE’s health technology appraisals Clarke, Sophie Ellis, Michelle Brownrigg, Jack Orphanet J Rare Dis Research BACKGROUND: In the absence of a framework designed to evaluate medicines for rare diseases in the UK, most orphan medicines are appraised by the National Institute for Health and Care Excellence (NICE) through the Single Technology Appraisal (STA) process. RESULTS: An analysis of STA appraisals of orphan and non-orphan medicines revealed that orphan medicines were subject to a significantly longer mean time in the NICE process than non-orphan medicines [370 days (n = 44) vs. 277 days (n = 118), p =  < 0.0001]. A higher proportion of orphan STAs required more than one Appraisal Committee Meeting (ACM) versus non-orphan STAs, and orphan STAs were disadvantaged by worse outcomes with respect to positive recommendations than those orphan medicines assessed by Highly Specialised Technology evaluation (HST). CONCLUSIONS: The uncertainties inherent to developing orphan medicines may contribute to these disadvantages. Improved understanding of the challenges in drug development for orphan medicines and clearer guidance for decision makers on navigating uncertainty in the HTA process may promote greater equity in access to medicines across rare and common conditions. BioMed Central 2021-05-13 /pmc/articles/PMC8117316/ /pubmed/33985575 http://dx.doi.org/10.1186/s13023-021-01845-x 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 Research
Clarke, Sophie
Ellis, Michelle
Brownrigg, Jack
The impact of rarity in NICE’s health technology appraisals
title The impact of rarity in NICE’s health technology appraisals
title_full The impact of rarity in NICE’s health technology appraisals
title_fullStr The impact of rarity in NICE’s health technology appraisals
title_full_unstemmed The impact of rarity in NICE’s health technology appraisals
title_short The impact of rarity in NICE’s health technology appraisals
title_sort impact of rarity in nice’s health technology appraisals
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8117316/
https://www.ncbi.nlm.nih.gov/pubmed/33985575
http://dx.doi.org/10.1186/s13023-021-01845-x
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