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The Danish model for the quick and safe implementation of infliximab and etanercept biosimilars

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European Journal of Clinical Pharmacology Aims and scope Submit manuscript

Abstract

Purpose

A rapidly increasing use of biological drugs has led to substantial costs. Shift to biosimilars enables considerable reduction of these costs without jeopardizing the treatment of patients, but most countries have extensive possibilities of untapped cost-savings. The aim of this study was to describe the Danish quick and near-complete implementation of the two first TNF inhibitor biosimilars (infliximab and etanercept).

Methods

We shed light on the considerations and experiences made during the implementation, and present key figures from the implementation.

Results

The infliximab biosimilar constituted 90.6% of the total amount of infliximab four months following patent expiration of the biooriginator. Similar results were seen for etanercept biosimilar. Substantial cost reductions were experienced in the way that e.g. the infliximab-shift reduced cost by two thirds.

Conclusion

We believe that a thorough preparation and an organizational setting supporting the implementation is crucial for the successful implementation. This same implementation model will be used for future biosimilars.

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Authors and Affiliations

Authors

Contributions

TBJ and HRC initiated this analysis. All authors work with rational pharmacotherapy in Denmark and cover all five Danish regions as well as the regional authorities’ pharmaceutical procurement service. DB, EAS, BKP, SEA, MMHC, LN, and HRC were key figures during the shift to biosimilars of infliximab and etanercept. TBJ, DB and HRC planned the analysis. TBJ analysed the data. All authors have critically revised the manuscript and approved the final version for publication. HRC stands as guarantor of the article. The corresponding author attests that all listed authors meet authorship criteria and that no other people meeting the criteria have been omitted.

Corresponding author

Correspondence to Thomas Bo Jensen.

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Pharmacoeconomics

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Jensen, T.B., Bartels, D., Sædder, E.A. et al. The Danish model for the quick and safe implementation of infliximab and etanercept biosimilars. Eur J Clin Pharmacol 76, 35–40 (2020). https://doi.org/10.1007/s00228-019-02765-3

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  • DOI: https://doi.org/10.1007/s00228-019-02765-3

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