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

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

DOI

  • Thomas Bo Jensen, Copenhagen University Hospital, Danmark
  • Dorthe Bartels, Amgros - The Regions’ Pharmaceutical Organisation, Danmark
  • Eva Aggerholm Sædder
  • Birgitte Klindt Poulsen, Aalborg Universitet, Danmark
  • Stig Ejdrup Andersen, Zealand University Hospital, Danmark
  • Mette Marie H Christensen, Syddansk Universitet, Danmark
  • Lars Nielsen, The Hospital Pharmacy of the Capital Region of Denmark
  • ,
  • Hanne Rolighed Christensen, Copenhagen University Hospital, Danmark
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.
OriginalsprogEngelsk
TidsskriftEuropean Journal of Clinical Pharmacology
Vol/bind76
Nummer1
Sider (fra-til)35-40
Antal sider6
ISSN0031-6970
DOI
StatusUdgivet - jan. 2020

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