Biological medicines are attracting attention from policymakers and health insurers across countries due to their increased financial burden. The potential for biosimilars’ cost savings can be influenced by various factors, including supply-side (pricing policies) and demand-side (usage-enhancing) policies.
Budget savings from biosimilar infliximab in the UK, France, Japan and Korea
Biosimilars/Research | Posted 11/09/2020 0 Post your comment
Kim and colleagues explored the market dynamics after the entry of biosimilar infliximab among four countries with (UK, France), and without (Japan, Korea) demand-side policies, using MIDAS-IQVIA data with 22 quarters of observational data up to March 2018 [1].
With the introduction of biosimilars, the sales value of infliximab increased approximately 2.5 times in Korea, whereas it only slightly increased (1.2 times for France and the UK) or decreased (0.9 times for Japan) in other countries. While stable market size dynamics were observed in the other countries, an escalating market size attributable to the increase in originator infliximab was observed in Korea. In the UK and France, which have implemented demand-side policies, the sales volume of originator infliximab appreciably decreased after the entry of biosimilar infliximab while that of biosimilars increased. However, in Korea, which has supply-side policies based on price-linking and few demand-side policies, the volume of originator infliximab actually increased by 70% alongside a very limited increase in biosimilar infliximab. The lowest price ratio between biosimilar and originator infliximab was found in Japan at 68%. In France and Korea, the ex-factory prices of biosimilar infliximab were 99% and 95%, respectively, of the originator infliximab price. In the UK, the ex-factory price of biosimilar infliximab started at 87% of that of originator infliximab and then decreased to 80% as the market matured. However, actual price differences might differ.
The authors suggested that the introduction of biosimilars actually increased financial burden in Korea and the government body should consider demand-side policy more heavily than supply-side policy to enhance cost-savings achieved by the introduction of the biosimilars in Korean context.
Conflict of interest
Authors of the research paper [1] reported conflict of interest, including being a founder of the KU Leuven Fund on Market Analysis of Biologics and Biosimilars following Loss of Exclusivity (MABEL), as well as being involved in a stakeholder roundtable and having contributed to studies on biologicals and biosimilars. For full details of the authors’ conflict of interest, see the research paper [1].
Abstracted by Yujeong Kim, Ewha Womans University, Seoul, South Korea.
Related article
How can EU policymakers access the potential of biosimilars
Reference
1. Kim Y, Kwon HY, Godman B, et al. Uptake of biosimilar infliximab in the UK, France, Japan, and Korea: budget savings or market expansion across countries?. Front Pharmacol. 2020;11:970.
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2020 Pro Pharma Communications International. All Rights Reserved
News
FDA approves fifth ustekinumab biosimilar Imuldosa
EC approval for three ustekinumab biosimilar: Eksunbi, Fymskina, Otulfi
General
SBR issues consensus on interchangeability of reference products and biosimilars
Innovative direct purchase agreement sees adalimumab biosimilar prices slashed
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
Long-term real-world safety experience of biosimilars confirms concept of biosimilarity
Budget impact analysis of Rixathon introduction in Chile for non-Hodgkin lymphoma
Biosimilars in inflammatory bowel disease: are we ready for multiple switches
Topline results from clinical development programme for candidate biosimilar AVT05 golimumab
Comments (0)
Post your comment