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Article

Key Drivers for Market Penetration of Biosimilars in Europe

by
Cécile Rémuzat
1,*,
Julie Dorey
2,
Olivier Cristeau
2,
Dan Ionescu
3,
Guerric Radière
3 and
Mondher Toumi
4
1
Pricing and Market Access Department, Creativ-Ceutical, Paris, France
2
HEOR Department, Creativ-Ceutical, Paris, France
3
Global Pricing and Market Access Biopharmaceuticals Department, Sandoz International GmbH, Holzkirchen, Germany
4
Faculté de Médecine, Laboratoire de Santé Publique, Aix-Marseille Université, Université de la Méditerranée, Marseille, France
*
Author to whom correspondence should be addressed.
J. Mark. Access Health Policy 2017, 5(1), 1272308; https://doi.org/10.1080/20016689.2016.1272308
Submission received: 1 January 2017 / Revised: 1 January 2017 / Accepted: 1 January 2017 / Published: 30 January 2017

Abstract

Background & Objectives: Potential drivers and barriers of biosimilar uptake were mainly analysed through qualitative approaches. The study objective was to conduct a quantitative analysis and identify drivers of biosimilar uptake of all available biosimilars in the European Union (EU). Methods: A three-step process was established to identify key drivers for the uptake of biosimilars in the top 10 EU member states (MS) pharmaceutical markets (Belgium, France, Germany, Greece, Hungary, Italy, Poland, Spain, Sweden, and the UK): (1) literature review to identify incentive policies in place to enhance biosimilars adoption; (2) assessment of biosimilar market dynamics based on database analysis; (3) regression model analysis on price using the following explicative variables: incentive policies; price difference between the biosimilar and the originator product; distribution channel; generic uptake and generic price cut; pharmaceutical expenditure per capita; and market competition. Results: At the study cut-off date, 20 biosimilars were available on the market. Incentive policies applied to biosimilars were found to be heterogeneous across countries, and uptakes of biosimilars were also very heterogeneous between different therapeutic classes and countries. Results from the model demonstrated that incentive policies and the date of first biosimilar market entry were correlated to biosimilar uptake. Pharmaceutical expenditure per capita and the highest generic uptake were inversely correlated with biosimilar uptake. Average generic price discount over originator and the number of biosimilars showed a trend toward statistical significance for correlation with biosimilar uptake, but did not reach the significance threshold. Biosimilar price discount over original biologic price, the number of analogues, and the distribution channel were not correlated with the biosimilar uptake. Conclusions: Understanding drivers of biosimilar uptake becomes a critical issue to inform policy decision-makers. This study showed that incentive policies to enhance uptake remain an important driver of biosimilar penetration, while biosimilar price discounts have no impact. Future research is warranted when the biosimilar market gains maturity.
Keywords: biosimilar; uptake; Europe; price erosion; market dynamics; incentive policies biosimilar; uptake; Europe; price erosion; market dynamics; incentive policies

Share and Cite

MDPI and ACS Style

Rémuzat, C.; Dorey, J.; Cristeau, O.; Ionescu, D.; Radière, G.; Toumi, M. Key Drivers for Market Penetration of Biosimilars in Europe. J. Mark. Access Health Policy 2017, 5, 1272308. https://doi.org/10.1080/20016689.2016.1272308

AMA Style

Rémuzat C, Dorey J, Cristeau O, Ionescu D, Radière G, Toumi M. Key Drivers for Market Penetration of Biosimilars in Europe. Journal of Market Access & Health Policy. 2017; 5(1):1272308. https://doi.org/10.1080/20016689.2016.1272308

Chicago/Turabian Style

Rémuzat, Cécile, Julie Dorey, Olivier Cristeau, Dan Ionescu, Guerric Radière, and Mondher Toumi. 2017. "Key Drivers for Market Penetration of Biosimilars in Europe" Journal of Market Access & Health Policy 5, no. 1: 1272308. https://doi.org/10.1080/20016689.2016.1272308

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