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The Pricing of Breakthrough Drugs: Theory and Policy Implications

Pharmaceutical sales exceed $850 billion a year, of which 84% are accounted for by brand drugs. Drug prices are the focus of an ongoing heated debate. While some argue that pharmaceutical companies exploit monopolistic power granted by patent protection to set prices that are “too high”, others clai...

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Detalles Bibliográficos
Autores principales: Levy, Moshe, Rizansky Nir, Adi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244177/
https://www.ncbi.nlm.nih.gov/pubmed/25422889
http://dx.doi.org/10.1371/journal.pone.0113894
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author Levy, Moshe
Rizansky Nir, Adi
author_facet Levy, Moshe
Rizansky Nir, Adi
author_sort Levy, Moshe
collection PubMed
description Pharmaceutical sales exceed $850 billion a year, of which 84% are accounted for by brand drugs. Drug prices are the focus of an ongoing heated debate. While some argue that pharmaceutical companies exploit monopolistic power granted by patent protection to set prices that are “too high”, others claim that these prices are necessary to motivate the high R&D investments required in the pharmaceutical industry. This paper employs a recently documented utility function of health and wealth to derive the theoretically optimal pricing of monopolistic breakthrough drugs. This model provides a framework for a quantitative discussion of drug price regulation. We show that mild price regulation can substantially increase consumer surplus and the number of patients who purchase the drug, while having only a marginal effect on the revenues of the pharmaceutical company.
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spelling pubmed-42441772014-12-05 The Pricing of Breakthrough Drugs: Theory and Policy Implications Levy, Moshe Rizansky Nir, Adi PLoS One Research Article Pharmaceutical sales exceed $850 billion a year, of which 84% are accounted for by brand drugs. Drug prices are the focus of an ongoing heated debate. While some argue that pharmaceutical companies exploit monopolistic power granted by patent protection to set prices that are “too high”, others claim that these prices are necessary to motivate the high R&D investments required in the pharmaceutical industry. This paper employs a recently documented utility function of health and wealth to derive the theoretically optimal pricing of monopolistic breakthrough drugs. This model provides a framework for a quantitative discussion of drug price regulation. We show that mild price regulation can substantially increase consumer surplus and the number of patients who purchase the drug, while having only a marginal effect on the revenues of the pharmaceutical company. Public Library of Science 2014-11-25 /pmc/articles/PMC4244177/ /pubmed/25422889 http://dx.doi.org/10.1371/journal.pone.0113894 Text en © 2014 Levy, Rizansky Nir http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Levy, Moshe
Rizansky Nir, Adi
The Pricing of Breakthrough Drugs: Theory and Policy Implications
title The Pricing of Breakthrough Drugs: Theory and Policy Implications
title_full The Pricing of Breakthrough Drugs: Theory and Policy Implications
title_fullStr The Pricing of Breakthrough Drugs: Theory and Policy Implications
title_full_unstemmed The Pricing of Breakthrough Drugs: Theory and Policy Implications
title_short The Pricing of Breakthrough Drugs: Theory and Policy Implications
title_sort pricing of breakthrough drugs: theory and policy implications
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4244177/
https://www.ncbi.nlm.nih.gov/pubmed/25422889
http://dx.doi.org/10.1371/journal.pone.0113894
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