Literature DB >> 24578185

Biosimilar granulocyte colony-stimulating factor uptakes in the EU-5 markets: a descriptive analysis.

François Bocquet1, Pascal Paubel, Isabelle Fusier, Anne-Laure Cordonnier, Claude Le Pen, Martine Sinègre.   

Abstract

BACKGROUND: Biosimilars are copies of biological reference medicines. Unlike generics (copies of chemical molecules), biologics are complex, expensive and complicated to produce. The knowledge of the factors affecting the competition following patent expiry for biologics remains limited.
OBJECTIVES: The aims of this study were to analyse the EU-5 Granulocyte-Colony Stimulating Factor (G-CSF) markets and to determine the factors affecting the G-CSF biosimilar uptakes, particularly that of biosimilar prices relative to originators.
METHODS: Data on medicine volumes, values, and ex-manufacturer prices for all G-CSF categories were provided by IMS Health. Volumes were calculated in defined daily doses (DDD) and prices in Euros per DDD. In the EU-5 countries, there is 5 years of experience with biosimilar G-CSFs (2007-2011).
RESULTS: Two G-CSF market profiles exist: (1) countries with a high retail market distribution, which are the largest G-CSF markets with low global G-CSF biosimilar uptakes (5.4% in France and 8.5% in Germany in 2011); and (2) countries with a dominant hospital channel, which are the smallest markets with higher G-CSF biosimilar uptakes (12.4% in Spain and 20.4% in the UK). The more the decisions are decentralized, the more their uptakes are high. The price difference between G-CSF biosimilars and their reference plays a marginal role at a global level (price differences of +13.3% in the UK and -20.4% in France).
CONCLUSION: The competition with G-CSF biosimilars varies significantly between EU-5 countries, probably because of G-CSF distribution channel differences. Currently, this competition is not mainly based on prices, but on local political options to stimulate tendering between them and recently branded second- or third-generation products.

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Year:  2014        PMID: 24578185     DOI: 10.1007/s40258-014-0087-8

Source DB:  PubMed          Journal:  Appl Health Econ Health Policy        ISSN: 1175-5652            Impact factor:   2.561


  11 in total

1.  Knowledge, behaviors and practices of community and hospital pharmacists towards biosimilar medicines: Results of a French web-based survey.

Authors:  Morgane Beck; Bruno Michel; Marie-Christine Rybarczyk-Vigouret; Dominique Levêque; Christelle Sordet; Jean Sibilia; Michel Velten
Journal:  MAbs       Date:  2016-12-08       Impact factor: 5.857

Review 2.  Pharmacoeconomics of Biosimilars: What Is There to Gain from Them?

Authors:  Filipe C Araújo; João Gonçalves; João Eurico Fonseca
Journal:  Curr Rheumatol Rep       Date:  2016-08       Impact factor: 4.592

3.  Competition Between Biosimilars and Patented Biologics: Learning from European and Japanese Experience.

Authors:  François Bocquet; Anaïs Loubière; Isabelle Fusier; Anne-Laure Cordonnier; Pascal Paubel
Journal:  Pharmacoeconomics       Date:  2016-11       Impact factor: 4.981

4.  Biosimilars in the USA: Will New Efforts to Spur Approvals and Access Spur Uptake and Cost Savings?

Authors:  Stanton R Mehr; Richard A Brook
Journal:  Pharmaceut Med       Date:  2019-02

5.  A multinational, drug utilization study of lipegfilgrastim use in real-world setting in Europe.

Authors:  Sigal Kaplan; Dana Ilic Bogojevic; Carolyn Rainville; Nicholas Gross
Journal:  Support Care Cancer       Date:  2022-08-31       Impact factor: 3.359

6.  Barriers to the uptake of biosimilars and possible solutions: a Belgian case study.

Authors:  Pieter Dylst; Arnold Vulto; Steven Simoens
Journal:  Pharmacoeconomics       Date:  2014-07       Impact factor: 4.981

Review 7.  Drug tendering: drug supply and shortage implications for the uptake of biosimilars.

Authors:  George Dranitsaris; Ira Jacobs; Carol Kirchhoff; Robert Popovian; Lesley G Shane
Journal:  Clinicoecon Outcomes Res       Date:  2017-09-29

8.  Supply-side and demand-side policies for biosimilars: an overview in 10 European member states.

Authors:  Cécile Rémuzat; Anna Kapuśniak; Aleksandra Caban; Dan Ionescu; Guerric Radière; Cyril Mendoza; Mondher Toumi
Journal:  J Mark Access Health Policy       Date:  2017-04-28

9.  Biosimilars: How Can Payers Get Long-Term Savings?

Authors:  Jorge Mestre-Ferrandiz; Adrian Towse; Mikel Berdud
Journal:  Pharmacoeconomics       Date:  2016-06       Impact factor: 4.981

Review 10.  Overcoming Barriers to the Market Access of Biosimilars in the European Union: The Case of Biosimilar Monoclonal Antibodies.

Authors:  Evelien Moorkens; Clara Jonker-Exler; Isabelle Huys; Paul Declerck; Steven Simoens; Arnold G Vulto
Journal:  Front Pharmacol       Date:  2016-06-29       Impact factor: 5.810

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