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The cost of multiple sclerosis drugs in the US and the pharmaceutical industry: Too big to fail?
OBJECTIVE: To examine the pricing trajectories in the United States of disease-modifying therapies (DMT) for multiple sclerosis (MS) over the last 20 years and assess the influences on rising prices. METHODS: We estimated the trend in annual drug costs for 9 DMTs using published drug pricing data fr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451044/ https://www.ncbi.nlm.nih.gov/pubmed/25911108 http://dx.doi.org/10.1212/WNL.0000000000001608 |
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author | Hartung, Daniel M. Bourdette, Dennis N. Ahmed, Sharia M. Whitham, Ruth H. |
author_facet | Hartung, Daniel M. Bourdette, Dennis N. Ahmed, Sharia M. Whitham, Ruth H. |
author_sort | Hartung, Daniel M. |
collection | PubMed |
description | OBJECTIVE: To examine the pricing trajectories in the United States of disease-modifying therapies (DMT) for multiple sclerosis (MS) over the last 20 years and assess the influences on rising prices. METHODS: We estimated the trend in annual drug costs for 9 DMTs using published drug pricing data from 1993 to 2013. We compared changes in DMT costs to general and prescription drug inflation during the same period. We also compared the cost trajectories for first-generation MS DMTs interferon (IFN)–β-1b, IFN-β-1a IM, and glatiramer acetate with contemporaneously approved biologic tumor necrosis factor (TNF) inhibitors. RESULTS: First-generation DMTs, originally costing $8,000 to $11,000, now cost about $60,000 per year. Costs for these agents have increased annually at rates 5 to 7 times higher than prescription drug inflation. Newer DMTs commonly entered the market with a cost 25%–60% higher than existing DMTs. Significant increases in the cost trajectory of the first-generation DMTs occurred following the Food and Drug Administration approvals of IFN-β-1a SC (2002) and natalizumab (reintroduced 2006) and remained high following introduction of fingolimod (2010). Similar changes did not occur with TNF inhibitor biologics during these time intervals. DMT costs in the United States currently are 2 to 3 times higher than in other comparable countries. CONCLUSIONS: MS DMT costs have accelerated at rates well beyond inflation and substantially above rates observed for drugs in a similar biologic class. There is an urgent need for clinicians, payers, and manufacturers in the United States to confront the soaring costs of DMTs. |
format | Online Article Text |
id | pubmed-4451044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-44510442015-06-15 The cost of multiple sclerosis drugs in the US and the pharmaceutical industry: Too big to fail? Hartung, Daniel M. Bourdette, Dennis N. Ahmed, Sharia M. Whitham, Ruth H. Neurology Contemporary Issues OBJECTIVE: To examine the pricing trajectories in the United States of disease-modifying therapies (DMT) for multiple sclerosis (MS) over the last 20 years and assess the influences on rising prices. METHODS: We estimated the trend in annual drug costs for 9 DMTs using published drug pricing data from 1993 to 2013. We compared changes in DMT costs to general and prescription drug inflation during the same period. We also compared the cost trajectories for first-generation MS DMTs interferon (IFN)–β-1b, IFN-β-1a IM, and glatiramer acetate with contemporaneously approved biologic tumor necrosis factor (TNF) inhibitors. RESULTS: First-generation DMTs, originally costing $8,000 to $11,000, now cost about $60,000 per year. Costs for these agents have increased annually at rates 5 to 7 times higher than prescription drug inflation. Newer DMTs commonly entered the market with a cost 25%–60% higher than existing DMTs. Significant increases in the cost trajectory of the first-generation DMTs occurred following the Food and Drug Administration approvals of IFN-β-1a SC (2002) and natalizumab (reintroduced 2006) and remained high following introduction of fingolimod (2010). Similar changes did not occur with TNF inhibitor biologics during these time intervals. DMT costs in the United States currently are 2 to 3 times higher than in other comparable countries. CONCLUSIONS: MS DMT costs have accelerated at rates well beyond inflation and substantially above rates observed for drugs in a similar biologic class. There is an urgent need for clinicians, payers, and manufacturers in the United States to confront the soaring costs of DMTs. Lippincott Williams & Wilkins 2015-05-26 /pmc/articles/PMC4451044/ /pubmed/25911108 http://dx.doi.org/10.1212/WNL.0000000000001608 Text en © 2015 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-Noncommercial No Derivative 3.0 License, which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Contemporary Issues Hartung, Daniel M. Bourdette, Dennis N. Ahmed, Sharia M. Whitham, Ruth H. The cost of multiple sclerosis drugs in the US and the pharmaceutical industry: Too big to fail? |
title | The cost of multiple sclerosis drugs in the US and the pharmaceutical industry: Too big to fail? |
title_full | The cost of multiple sclerosis drugs in the US and the pharmaceutical industry: Too big to fail? |
title_fullStr | The cost of multiple sclerosis drugs in the US and the pharmaceutical industry: Too big to fail? |
title_full_unstemmed | The cost of multiple sclerosis drugs in the US and the pharmaceutical industry: Too big to fail? |
title_short | The cost of multiple sclerosis drugs in the US and the pharmaceutical industry: Too big to fail? |
title_sort | cost of multiple sclerosis drugs in the us and the pharmaceutical industry: too big to fail? |
topic | Contemporary Issues |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451044/ https://www.ncbi.nlm.nih.gov/pubmed/25911108 http://dx.doi.org/10.1212/WNL.0000000000001608 |
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