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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

Authors :
Evelien Moorkens
Brian Godman
Isabelle Huys
Iris Hoxha
Admir Malaj
Simon Keuerleber
Silvia Stockinger
Sarah Mörtenhuber
Maria Dimitrova
Konstantin Tachkov
Luka Vončina
Vera Vlahović Palčevski
Gnosia Achniotou
Juraj Slabý
Leona Popelková
Kateřina Kohoutová
Dorthe Bartels
Ott Laius
Jaana E. Martikainen
Gisbert W. Selke
Vasileios Kourafalos
Einar Magnússon
Rannveig Einarsdóttir
Roisín Adams
Roberta Joppi
Eleonora Allocati
Arianit Jakupi
Anita Viksna
Ieva Greičiūtė-Kuprijanov
Patricia Vella Bonanno
Vincent Suttorp
Øyvind Melien
Robert Plisko
Ileana Mardare
Dmitry Meshkov
Tanja Novakovic
Jurij Fürst
Corinne Zara
Vanda Marković-Peković
Nataša Grubiša
Gustaf Befrits
Robert Puckett
Arnold G. Vulto
Source :
Frontiers in Pharmacology, Vol 11 (2021)
Publication Year :
2021
Publisher :
Frontiers Media S.A., 2021.

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.

Details

Language :
English
ISSN :
16639812
Volume :
11
Database :
Directory of Open Access Journals
Journal :
Frontiers in Pharmacology
Publication Type :
Academic Journal
Accession number :
edsdoj.91efa0738a404ac58954a5cf23bc3c10
Document Type :
article
Full Text :
https://doi.org/10.3389/fphar.2020.591134