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Launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries
BACKGROUND: New medicines are increasingly being identified as efficacious across multiple indications. The impact of current pricing and reimbursement policies on launch decisions across these indications remains unclear. OBJECTIVE: This paper, first, maps marketing authorisation and HTA coverage r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923892/ https://www.ncbi.nlm.nih.gov/pubmed/36782175 http://dx.doi.org/10.1186/s12913-023-09095-2 |
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author | Mills, Mackenzie Michaeli, Daniel Miracolo, Aurelio Kanavos, Panos |
author_facet | Mills, Mackenzie Michaeli, Daniel Miracolo, Aurelio Kanavos, Panos |
author_sort | Mills, Mackenzie |
collection | PubMed |
description | BACKGROUND: New medicines are increasingly being identified as efficacious across multiple indications. The impact of current pricing and reimbursement policies on launch decisions across these indications remains unclear. OBJECTIVE: This paper, first, maps marketing authorisation and HTA coverage recommendation sequences of multi-indication medicines across Germany, France, England, Scotland, Canada, Australia, and the USA, and, second, evaluates the clinical characteristics, clinical development time and coverage recommendation time of multi-indication medicines, drawing comparisons between the first and subsequent indications of an approved molecule. METHODS: Medicine approvals by the Food and Drug Administration between 2009–2019 were screened to identify multi-indication products with approved oncology indications. Data on clinical trial characteristics, clinical performance and HTA outcomes were extracted from publicly available regulatory approval and HTA reports. RESULTS: Relative to subsequent indications, first indications were more likely to receive conditional marketing authorisation, have an orphan designation, have a single arm phase II pivotal trial and lower MCBS score. Subsequent indications had faster HTA coverage recommendation times in England and Canada. While the majority of first indications received HTA coverage recommendations across all settings, the proportion of subsequent indications with HTA coverage recommendations was lower and uptake varied considerably across settings. CONCLUSIONS: Discordance in the value of first versus subsequent indications can pose major challenges in systems that define price based on the initial indication. Current pricing and reimbursement systems generate significant fragmentation in the approval and availability of multi-indication products across settings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12913-023-09095-2. |
format | Online Article Text |
id | pubmed-9923892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99238922023-02-14 Launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries Mills, Mackenzie Michaeli, Daniel Miracolo, Aurelio Kanavos, Panos BMC Health Serv Res Research BACKGROUND: New medicines are increasingly being identified as efficacious across multiple indications. The impact of current pricing and reimbursement policies on launch decisions across these indications remains unclear. OBJECTIVE: This paper, first, maps marketing authorisation and HTA coverage recommendation sequences of multi-indication medicines across Germany, France, England, Scotland, Canada, Australia, and the USA, and, second, evaluates the clinical characteristics, clinical development time and coverage recommendation time of multi-indication medicines, drawing comparisons between the first and subsequent indications of an approved molecule. METHODS: Medicine approvals by the Food and Drug Administration between 2009–2019 were screened to identify multi-indication products with approved oncology indications. Data on clinical trial characteristics, clinical performance and HTA outcomes were extracted from publicly available regulatory approval and HTA reports. RESULTS: Relative to subsequent indications, first indications were more likely to receive conditional marketing authorisation, have an orphan designation, have a single arm phase II pivotal trial and lower MCBS score. Subsequent indications had faster HTA coverage recommendation times in England and Canada. While the majority of first indications received HTA coverage recommendations across all settings, the proportion of subsequent indications with HTA coverage recommendations was lower and uptake varied considerably across settings. CONCLUSIONS: Discordance in the value of first versus subsequent indications can pose major challenges in systems that define price based on the initial indication. Current pricing and reimbursement systems generate significant fragmentation in the approval and availability of multi-indication products across settings. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12913-023-09095-2. BioMed Central 2023-02-13 /pmc/articles/PMC9923892/ /pubmed/36782175 http://dx.doi.org/10.1186/s12913-023-09095-2 Text en © The Author(s) 2023 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 Mills, Mackenzie Michaeli, Daniel Miracolo, Aurelio Kanavos, Panos Launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries |
title | Launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries |
title_full | Launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries |
title_fullStr | Launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries |
title_full_unstemmed | Launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries |
title_short | Launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries |
title_sort | launch sequencing of pharmaceuticals with multiple therapeutic indications: evidence from seven countries |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923892/ https://www.ncbi.nlm.nih.gov/pubmed/36782175 http://dx.doi.org/10.1186/s12913-023-09095-2 |
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