Analysis of biosimilars consumption in an Italian Local Health Authority
- PMID: 38231416
- DOI: 10.1007/s00210-024-02951-w
Analysis of biosimilars consumption in an Italian Local Health Authority
Abstract
Biosimilar drugs offer an opportunity for all global healthcare systems because they provide significant cost savings while ensuring equal efficacy and safety in the treatment of chronic diseases. These savings can be allocated to support ongoing innovation. An analysis of the usage of major biosimilar drugs across various therapeutic areas has been conducted within an Italian healthcare company serving a population of over one million. Data on consumption, expenditure, and the number of treated patients has been extracted from the company's databases. Finally, a comparison with the year 2021 has been performed to determine if biosimilar drug usage increased in 2022. In 2022, the data reveals that a substantial portion of the analysed active ingredients are being used as biosimilar drugs, except in a few residual cases. However, among the most consumed drugs, resistance still exists in the case of Adalimumab and Etanercept, for which expenditure on originator drugs exceeds 2 million euros. The 2022-2021 comparison highlights the increasing use of biosimilar drugs. This data is encouraging and suggests that in the coming months, we may achieve total utilization, which would be to the benefit of the National Healthcare System (NHS) and the citizens who can rely on an efficient and sustainable healthcare policy that is continually improving.
Keywords: Biological drugs; Biosimilars; Biotechnological; Cost-containment strategies; Pharmaceuticals; Proteins; Sustainability; Therapeutic.
© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
References
-
- Abitbol V, Benkhalifa S, Habauzit C, Marotte H (2023) Navigating adalimumab biosimilars: an expert opinion. J Comp Eff Res. 12(11):e230117. https://doi.org/10.57264/cer-2023-0117 - DOI - PubMed - PMC
-
- Capuozzo M, Nava E, Cascone S, Cinque C, Marra R, Ottaiano A, Scognamiglio C, Palumbo E (2013) Assessment of expenditure control and prescriptive appropriateness of biological drugs in autoimmune diseases and chronic inflammatory bowel disease. Front Pharmacol 22(4):31. https://doi.org/10.3389/fphar.2013.00031 - DOI
-
- Capuozzo M, Celotto V, Zovi A, Langella R, Ferrara F (2023) Recovery of suspended reimbursements of high-cost drugs subjected to monitoring registries and negotiated agreements (MEAs): a tool for governance and clinical appropriateness in the Italian reality. Eur J Health Econ. https://doi.org/10.1007/s10198-023-01640-4 - DOI - PubMed
-
- Chin WW (2015) A delicate balance—pharmaceutical innovation and access. N Engl J Med. 373(19):1799–801. https://doi.org/10.1056/NEJMp1513227 - DOI - PubMed
-
- Curto S, Ghislandi S, van de Vooren K, Duranti S, Garattini L (2014) Regional tenders on biosimilars in Italy: an empirical analysis of awarded prices. Health Policy 116(2–3):182–187. https://doi.org/10.1016/j.healthpol.2014.02.011 - DOI - PubMed
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