Evidence map›Paper›PMID 41296238›Full record

ArticleHealth economics review2025

Horizon scanning and drug expenditure for rare diseases: three-year predictive model in Italy 2025-2027.

Andrea Marcellusi, Daniela Cazzato, Giulio Guarnotta, Andrea Aiello, Marzia Bonfanti, Rossella Bitonti, Melissa Guardigni, Chiara Lucchetti, Fulvio Luccini, Pier Luigi Canonico and 1 more

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Article in Health economics review, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Andrea MarcellusiDepartment of Pharmaceutical Science (DISFARM), University of Milan, Milan, Italy.
Daniela CazzatoDepartment of Economics, Economic Evaluation and HTA (EEHTA-CEIS), University of Rome "Tor Vergata", Roma, 00133, Italy.
Giulio GuarnottaDepartment of Economics, Economic Evaluation and HTA (EEHTA-CEIS), University of Rome "Tor Vergata", Roma, 00133, Italy. giulio.guarnotta@uniroma2.it.
Andrea AielloPharmaLex Italy S.p.A, Milan, Italy.
Marzia BonfantiPharmaLex Italy S.p.A, Milan, Italy.
Rossella BitontiPharmaLex Italy S.p.A, Milan, Italy.
Melissa GuardigniPharmaLex Italy S.p.A, Milan, Italy.
Chiara LucchettiPharmaLex Italy S.p.A, Milan, Italy.
Fulvio LucciniPharmaLex Italy S.p.A, Milan, Italy.
Pier Luigi CanonicoDepartment of Pharmaceutical Sciences, University of Eastern Piedmont "Amedeo Avogadro", Vercelli, Italy.
Claudio JommiDepartment of Pharmaceutical Sciences, University of Eastern Piedmont "Amedeo Avogadro", Vercelli, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveIn recent years, spending on orphan drugs in Italy has seen a significant rise. The analysis aims to estimate future spending for medicines for rare diseases (RDs) in Italy.

methodsA forecasting model was developed over a three-year time frame. New drugs were selected according to specific criteria, using Biomedtracker and clinical trial databases. For each therapeutic indication, comparators were identified to estimate the average cost per patient. Overall expenditure was projected by applying prevalence data to the eligible population, and considering expected drug uptake trends over the study period. Additionally, a deterministic sensitivity analysis was performed to assess the influence of price fluctuations on total pharmaceutical spending.

resultsOverall, a total of 137 pipeline drugs for RDs were identified, covering 74 indications. The model estimated a total spending on RD treatments equal to €2.08 billion in 2024, corresponding to an average cost of €24,777 per patient. The projection indicates an increase by 1.9% in 2025, 4.0% in 2026, and 7.1% in 2027 compared to 2024. Focusing on orphan designation drugs (n = 115), the 2024 expenditure was estimated at €1.93 billion, with an average patient cost of €22,984. The introduction of new orphan drugs is expected to drive further increases in spending by 1.1% in 2025, 2.2% in 2026, and 3.7% in 2027.

conclusionsThe results underscore the growing financial impact of orphan drugs on Italy's healthcare budget. This analysis offers a quantitative projection of the resources required to ensure continued access to innovative therapies for RDs.

Indexed as

Forecast modelHorizon scanningOrphan drugsPharmaceutical expenditureRare diseases

Identifiers

PMID41296238
PMCPMC12751663

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.