Capture réglementaire en temps de pandémie

In the midst of the covid-19 pandemic, the Food and Drug Administration (FDA) published in March the orphan drug status granted to remdesivir, a molecule patented by Gilead as a treatment for the new coronavirus. This gave the company seven years of market exclusivity for its drug in the US market....

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Main Author: Samira Guennif
Format: Article
Language:English
Published: Association Recherche & Régulation 2021-02-01
Series:Revue de la Régulation
Subjects:
Online Access:https://journals.openedition.org/regulation/17621
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author Samira Guennif
author_facet Samira Guennif
author_sort Samira Guennif
collection DOAJ
description In the midst of the covid-19 pandemic, the Food and Drug Administration (FDA) published in March the orphan drug status granted to remdesivir, a molecule patented by Gilead as a treatment for the new coronavirus. This gave the company seven years of market exclusivity for its drug in the US market. This decision was immediately denounced as a clear misuse of the Orphan Drug Act (ODA) administered by the FDA under the influence of the pharmaceutical industry; a case of regulatory capture. The purpose of this article is to explore the concept of regulatory capture, drawing on work developed in the field of political science and (international) political economy, and based on the case study of remdesivir. It is shown that there have been multiple captures around a public good: agency, statutory, corrosive or cultural captures, to draw on the work of Carpenter (2014) developed in a break with those of economic regulation theory. Finally, recommendations are made to strengthen the ODA and limit its vulnerability to capture.
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spelling doaj-art-7d86779126ee44e5aa9b2a73edb858172025-01-30T14:25:57ZengAssociation Recherche & RégulationRevue de la Régulation1957-77962021-02-012910.4000/regulation.17621Capture réglementaire en temps de pandémieSamira GuennifIn the midst of the covid-19 pandemic, the Food and Drug Administration (FDA) published in March the orphan drug status granted to remdesivir, a molecule patented by Gilead as a treatment for the new coronavirus. This gave the company seven years of market exclusivity for its drug in the US market. This decision was immediately denounced as a clear misuse of the Orphan Drug Act (ODA) administered by the FDA under the influence of the pharmaceutical industry; a case of regulatory capture. The purpose of this article is to explore the concept of regulatory capture, drawing on work developed in the field of political science and (international) political economy, and based on the case study of remdesivir. It is shown that there have been multiple captures around a public good: agency, statutory, corrosive or cultural captures, to draw on the work of Carpenter (2014) developed in a break with those of economic regulation theory. Finally, recommendations are made to strengthen the ODA and limit its vulnerability to capture.https://journals.openedition.org/regulation/17621pharmaceutical industrypublic healthpandemicmedicineregulatory capture
spellingShingle Samira Guennif
Capture réglementaire en temps de pandémie
Revue de la Régulation
pharmaceutical industry
public health
pandemic
medicine
regulatory capture
title Capture réglementaire en temps de pandémie
title_full Capture réglementaire en temps de pandémie
title_fullStr Capture réglementaire en temps de pandémie
title_full_unstemmed Capture réglementaire en temps de pandémie
title_short Capture réglementaire en temps de pandémie
title_sort capture reglementaire en temps de pandemie
topic pharmaceutical industry
public health
pandemic
medicine
regulatory capture
url https://journals.openedition.org/regulation/17621
work_keys_str_mv AT samiraguennif capturereglementaireentempsdepandemie