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The Expiry of Humira® Market Exclusivity and the Entry of Adalimumab Biosimilars in Europe: An Overview of Pricing and National Policy Measures

Evelien Moorkens 1
Brian Godman 2, 3, 4
Isabelle HUYS 1
Iris Hoxha 5
Admir Malaj 5
Simon Keuerleber 6
Silvia Stockinger 6
Sarah Mörtenhuber 6
Maria Dimitrova 7
Konstantin Tachkov 7
Luka Vončina 8
Vera Vlahović Palčevski 8
Gnosia Achniotou 9
Juraj Slabý 10
Leona Popelková 10
Kateřina Kohoutová 10
Dorthe Bartels 11
Ott Laius 12
Jaana E. Martikainen 13
Gisbert W Selke 14
Vasileios Kourafalos 15
Einar Magnússon 16
Rannveig Einarsdóttir 17
Roisín Adams 18
Roberta Joppi 19
Eleonora Allocati 20
Arianit Jakupi 21
Anita Viksna 22
Ieva Greičiūtė Kuprijanov 23
Patricia Vella Bonanno 2
Vincent Suttorp 24
Øyvind Melien 25
Robert Plisko 26
Ileana Mardare 27
Dmitry Meshkov 28
Tanja Novakovic 29
Jurij Fürst 30
Corinne Zara 31
Vanda Marković Peković 32
Nataša Grubiša 33
Gustaf Befrits 34
Robert Puckett 35
Arnold G. Vulto 1, 24
6
 
Austrian Social Insurance, Austria
9
 
Health Insurance Organization (HIO), Cyprus
10
 
State Institute for Drug Control, Czechia
11
 
Amgros, Denmark
12
 
State Agency of Medicines, Estonia
13
 
Pharmaceuticals Pricing Board, Ministry of Social Affairs and Health, Finland
14
 
AOK Research Institute (WIdO), Germany
15
 
National Organization for the Provision of Healthcare Services (EOPYY), Greece
16
 
Ministry of Welfare, Iceland
19
 
Clinical Research and Drug Evaluation Unit, Local Health Authority of Verona, Italy
21
 
UBT ? Higher Education Institute, Kosovo
22
 
Department of Medicines and Medical Devices, The National Health Service, Latvia
23
 
Ministry of Health of the Republic of Lithuania, Lithuania
26
 
HTA Consulting, Poland
29
 
ZEM Solutions, Serbia
30
 
Health Insurance Institute, Slovenia
31
 
Drug Area, Catalan Health Service, Spain
33
 
Health Insurance Fund, Bosnia and Herzegovina
34
 
Stockholm County Council, Sweden
Publication typeJournal Article
Publication date2021-01-08
scimago Q1
wos Q1
SJR1.220
CiteScore8.9
Impact factor4.8
ISSN16639812
Pharmacology
Pharmacology (medical)
Abstract

Background: From October 2018, adalimumab biosimilars could enter the European market. However, in some countries, such as Netherlands, high discounts reported for the originator product may have influenced biosimilar entry.

Objectives: The aim of this paper is to provide a European overview of (list) prices of originator adalimumab, before and after loss of exclusivity; to report changes in the reimbursement status of adalimumab products; and discuss relevant policy measures.

Methods: Experts in European countries received a survey consisting of three parts: 1) general financing/co-payment of medicines, 2) reimbursement status and prices of originator adalimumab, and availability of biosimilars, and 3) policy measures related to the use of adalimumab.

Results: In May 2019, adalimumab biosimilars were available in 24 of the 30 countries surveyed. Following introduction of adalimumab biosimilars, a number of countries have made changes in relation to the reimbursement status of adalimumab products. Originator adalimumab list prices varied between countries by a factor of 2.8 before and 4.1 after loss of exclusivity. Overall, list prices of originator adalimumab decreased after loss of exclusivity, although for 13 countries list prices were unchanged. When reported, discounts/rebates on originator adalimumab after loss of exclusivity ranged from 0% to approximately 26% (Romania), 60% (Poland), 80% (Denmark, Italy, Norway), and 80–90% (Netherlands), leading to actual prices per pen or syringe between €412 (Finland) and €50 – €99 (Netherlands). To leverage competition following entry of biosimilar adalimumab, only a few countries adopted measures specifically for adalimumab in addition to general policies regarding biosimilars. In some countries, a strategy was implemented even before loss of exclusivity (Denmark, Scotland), while others did not report specific measures.

Conclusion: Even though originator adalimumab is the highest selling product in the world, few countries have implemented specific policies and practices for (biosimilar) adalimumab. Countries with biosimilars on the market seem to have competition lowering list or actual prices. Reported discounts varied widely between countries.

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GOST Copy
Moorkens E. et al. The Expiry of Humira® Market Exclusivity and the Entry of Adalimumab Biosimilars in Europe: An Overview of Pricing and National Policy Measures // Frontiers in Pharmacology. 2021. Vol. 11.
GOST all authors (up to 50) Copy
Moorkens E., Godman B., HUYS I., Hoxha I., Malaj A., Keuerleber S., Stockinger S., Mörtenhuber S., Dimitrova M., Tachkov K., Vončina L., Palčevski V. V., Achniotou G., Slabý J., Popelková L., Kohoutová K., Bartels D., Laius O., Martikainen J. E., Selke G. W., Kourafalos V., Magnússon E., Einarsdóttir R., Adams R., Joppi R., Allocati E., Jakupi A., Viksna A., Greičiūtė Kuprijanov I., Vella Bonanno P., Suttorp V., Melien Ø., Plisko R., Mardare I., Meshkov D., Novakovic T., Fürst J., Zara C., Marković Peković V., Grubiša N., Befrits G., Puckett R., Vulto A. G. The Expiry of Humira® Market Exclusivity and the Entry of Adalimumab Biosimilars in Europe: An Overview of Pricing and National Policy Measures // Frontiers in Pharmacology. 2021. Vol. 11.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.3389/fphar.2020.591134
UR - https://doi.org/10.3389/fphar.2020.591134
TI - The Expiry of Humira® Market Exclusivity and the Entry of Adalimumab Biosimilars in Europe: An Overview of Pricing and National Policy Measures
T2 - Frontiers in Pharmacology
AU - Moorkens, Evelien
AU - Godman, Brian
AU - HUYS, Isabelle
AU - Hoxha, Iris
AU - Malaj, Admir
AU - Keuerleber, Simon
AU - Stockinger, Silvia
AU - Mörtenhuber, Sarah
AU - Dimitrova, Maria
AU - Tachkov, Konstantin
AU - Vončina, Luka
AU - Palčevski, Vera Vlahović
AU - Achniotou, Gnosia
AU - Slabý, Juraj
AU - Popelková, Leona
AU - Kohoutová, Kateřina
AU - Bartels, Dorthe
AU - Laius, Ott
AU - Martikainen, Jaana E.
AU - Selke, Gisbert W
AU - Kourafalos, Vasileios
AU - Magnússon, Einar
AU - Einarsdóttir, Rannveig
AU - Adams, Roisín
AU - Joppi, Roberta
AU - Allocati, Eleonora
AU - Jakupi, Arianit
AU - Viksna, Anita
AU - Greičiūtė Kuprijanov, Ieva
AU - Vella Bonanno, Patricia
AU - Suttorp, Vincent
AU - Melien, Øyvind
AU - Plisko, Robert
AU - Mardare, Ileana
AU - Meshkov, Dmitry
AU - Novakovic, Tanja
AU - Fürst, Jurij
AU - Zara, Corinne
AU - Marković Peković, Vanda
AU - Grubiša, Nataša
AU - Befrits, Gustaf
AU - Puckett, Robert
AU - Vulto, Arnold G.
PY - 2021
DA - 2021/01/08
PB - Frontiers Media S.A.
VL - 11
PMID - 33519450
SN - 1663-9812
ER -
BibTex
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BibTex (up to 50 authors) Copy
@article{2021_Moorkens,
author = {Evelien Moorkens and Brian Godman and Isabelle HUYS and Iris Hoxha and Admir Malaj and Simon Keuerleber and Silvia Stockinger and Sarah Mörtenhuber and Maria Dimitrova and Konstantin Tachkov and Luka Vončina and Vera Vlahović Palčevski and Gnosia Achniotou and Juraj Slabý and Leona Popelková and Kateřina Kohoutová and Dorthe Bartels and Ott Laius and Jaana E. Martikainen and Gisbert W Selke and Vasileios Kourafalos and Einar Magnússon and Rannveig Einarsdóttir and Roisín Adams and Roberta Joppi and Eleonora Allocati and Arianit Jakupi and Anita Viksna and Ieva Greičiūtė Kuprijanov and Patricia Vella Bonanno and Vincent Suttorp and Øyvind Melien and Robert Plisko and Ileana Mardare and Dmitry Meshkov and Tanja Novakovic and Jurij Fürst and Corinne Zara and Vanda Marković Peković and Nataša Grubiša and Gustaf Befrits and Robert Puckett and Arnold G. Vulto},
title = {The Expiry of Humira® Market Exclusivity and the Entry of Adalimumab Biosimilars in Europe: An Overview of Pricing and National Policy Measures},
journal = {Frontiers in Pharmacology},
year = {2021},
volume = {11},
publisher = {Frontiers Media S.A.},
month = {jan},
url = {https://doi.org/10.3389/fphar.2020.591134},
doi = {10.3389/fphar.2020.591134}
}