Cargando…
The role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic R&D: a qualitative study
BACKGROUND: Few antibiotics have entered the market in recent years despite the need for new treatment options. Some of the challenges of bringing new antibiotics to market are linked to the marketing authorization and health technology assessment (HTA) processes. Research shows great variation in g...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045501/ https://www.ncbi.nlm.nih.gov/pubmed/36973761 http://dx.doi.org/10.1186/s40545-023-00556-x |
_version_ | 1784913618842681344 |
---|---|
author | Kållberg, Cecilia Mathiesen, Liv Gopinathan, Unni Salvesen Blix, Hege |
author_facet | Kållberg, Cecilia Mathiesen, Liv Gopinathan, Unni Salvesen Blix, Hege |
author_sort | Kållberg, Cecilia |
collection | PubMed |
description | BACKGROUND: Few antibiotics have entered the market in recent years despite the need for new treatment options. Some of the challenges of bringing new antibiotics to market are linked to the marketing authorization and health technology assessment (HTA) processes. Research shows great variation in geographic availability of new antibiotics, suggesting that market introduction of new antibiotics is unpredictable. We aimed to investigate regulatory authorities’ and HTA agencies’ role in developing non-financial incentives to stimulate antibiotic research and development (R&D). METHODS: We conducted individual, semi-structured, stakeholder interviews. Participants were recruited from regulatory authorities (EMA and FDA) and HTA agencies in Europe. Participants had to be experienced with assessment of antibiotics. The data were analyzed using a deductive and inductive approach to develop codes and identify key themes. Data were analyzed using thematic analysis including the constant comparison method to define concepts, and rival thinking to identify alternative explanations. RESULTS: We found that (1) interpretation of key concepts guiding the understanding of what type of antibiotics are needed vary (2) lack of a shared approach on how to deal with limited clinical data in the marketing authorization and HTA processes is causing barriers to getting new antibiotics to market (3) necessary adaptations to the marketing authorization process causes uncertainties that transmit to other key stakeholders involved in delivering antibiotics to patients. CONCLUSIONS: A shared understanding of limited clinical data and how to deal with this issue is needed amongst stakeholders involved in antibiotic R&D, marketing authorization, and market introduction to ensure antibiotics reach the market before resistance levels are out of control. Regulatory authorities and HTA agencies could play an active role in aligning the view of what constitutes an unmet medical need, and direct new economic models towards stimulating greater diversity in the antibiotic armamentarium. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40545-023-00556-x. |
format | Online Article Text |
id | pubmed-10045501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100455012023-03-29 The role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic R&D: a qualitative study Kållberg, Cecilia Mathiesen, Liv Gopinathan, Unni Salvesen Blix, Hege J Pharm Policy Pract Research BACKGROUND: Few antibiotics have entered the market in recent years despite the need for new treatment options. Some of the challenges of bringing new antibiotics to market are linked to the marketing authorization and health technology assessment (HTA) processes. Research shows great variation in geographic availability of new antibiotics, suggesting that market introduction of new antibiotics is unpredictable. We aimed to investigate regulatory authorities’ and HTA agencies’ role in developing non-financial incentives to stimulate antibiotic research and development (R&D). METHODS: We conducted individual, semi-structured, stakeholder interviews. Participants were recruited from regulatory authorities (EMA and FDA) and HTA agencies in Europe. Participants had to be experienced with assessment of antibiotics. The data were analyzed using a deductive and inductive approach to develop codes and identify key themes. Data were analyzed using thematic analysis including the constant comparison method to define concepts, and rival thinking to identify alternative explanations. RESULTS: We found that (1) interpretation of key concepts guiding the understanding of what type of antibiotics are needed vary (2) lack of a shared approach on how to deal with limited clinical data in the marketing authorization and HTA processes is causing barriers to getting new antibiotics to market (3) necessary adaptations to the marketing authorization process causes uncertainties that transmit to other key stakeholders involved in delivering antibiotics to patients. CONCLUSIONS: A shared understanding of limited clinical data and how to deal with this issue is needed amongst stakeholders involved in antibiotic R&D, marketing authorization, and market introduction to ensure antibiotics reach the market before resistance levels are out of control. Regulatory authorities and HTA agencies could play an active role in aligning the view of what constitutes an unmet medical need, and direct new economic models towards stimulating greater diversity in the antibiotic armamentarium. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40545-023-00556-x. BioMed Central 2023-03-27 /pmc/articles/PMC10045501/ /pubmed/36973761 http://dx.doi.org/10.1186/s40545-023-00556-x 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 Kållberg, Cecilia Mathiesen, Liv Gopinathan, Unni Salvesen Blix, Hege The role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic R&D: a qualitative study |
title | The role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic R&D: a qualitative study |
title_full | The role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic R&D: a qualitative study |
title_fullStr | The role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic R&D: a qualitative study |
title_full_unstemmed | The role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic R&D: a qualitative study |
title_short | The role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic R&D: a qualitative study |
title_sort | role of drug regulatory authorities and health technology assessment agencies in shaping incentives for antibiotic r&d: a qualitative study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045501/ https://www.ncbi.nlm.nih.gov/pubmed/36973761 http://dx.doi.org/10.1186/s40545-023-00556-x |
work_keys_str_mv | AT kallbergcecilia theroleofdrugregulatoryauthoritiesandhealthtechnologyassessmentagenciesinshapingincentivesforantibioticrdaqualitativestudy AT mathiesenliv theroleofdrugregulatoryauthoritiesandhealthtechnologyassessmentagenciesinshapingincentivesforantibioticrdaqualitativestudy AT gopinathanunni theroleofdrugregulatoryauthoritiesandhealthtechnologyassessmentagenciesinshapingincentivesforantibioticrdaqualitativestudy AT salvesenblixhege theroleofdrugregulatoryauthoritiesandhealthtechnologyassessmentagenciesinshapingincentivesforantibioticrdaqualitativestudy AT kallbergcecilia roleofdrugregulatoryauthoritiesandhealthtechnologyassessmentagenciesinshapingincentivesforantibioticrdaqualitativestudy AT mathiesenliv roleofdrugregulatoryauthoritiesandhealthtechnologyassessmentagenciesinshapingincentivesforantibioticrdaqualitativestudy AT gopinathanunni roleofdrugregulatoryauthoritiesandhealthtechnologyassessmentagenciesinshapingincentivesforantibioticrdaqualitativestudy AT salvesenblixhege roleofdrugregulatoryauthoritiesandhealthtechnologyassessmentagenciesinshapingincentivesforantibioticrdaqualitativestudy |