Evidence map›Paper›PMID 42479353›Full record

ArticleThe European journal of health economics : HEPAC : health economics in prevention and care2026

Closing the first wave of drug innovativeness in italy: final evidence from 2017 to 2025.

Giorgio Casilli, Carlotta Galeone, Marika De Nigris, Armando A Genazzani, Patrizia Popoli, Andrea Marcellusi, Dario Lidonnici, Claudio Jommi

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Article in The European journal of health economics : HEPAC : health economics in prevention and care, 2026. 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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Giorgio CasilliDepartment of Drug Science and Technology, University of Turin, Turin, Italy. giorgio.casilli@unito.it.ORCID http://orcid.org/0000-0001-5181-5099
Carlotta GaleoneBicocca Applied Statistics Center (B-ASC), University of Milano-Bicocca, Milan, Italy.ORCID http://orcid.org/0000-0003-1934-5167
Marika De NigrisMore Than Access (MTA) Srl SB, Milan, Italy.ORCID http://orcid.org/0009-0009-2224-3840
Armando A GenazzaniDepartment of Drug Science and Technology, University of Turin, Turin, Italy.ORCID http://orcid.org/0000-0003-1923-7430
Patrizia PopoliFormerly Director of the National Center of Drug Evaluation, Istituto Superiore di Sanità (ISS), Rome, Italy.ORCID http://orcid.org/0000-0002-9064-0639
Andrea MarcellusiDepartment of Pharmaceutical Sciences, University of Milan, Milan, Italy.ORCID http://orcid.org/0000-0002-3974-3798
Dario LidonniciMore Than Access (MTA) Srl SB, Milan, Italy.ORCID http://orcid.org/0000-0003-3136-0327
Claudio JommiDepartment of Pharmaceutical Sciences, Università del Piemonte Orientale "Amedeo Avogadro", Novara, Italy.ORCID http://orcid.org/0000-0002-2862-2990

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study provides a comprehensive overview of the Italian framework for the appraisal of drug innovativeness, covering all 294 appraisals conducted by AIFA between 2017 and June 2025. It aims to describe the evolution and application of the 2017 criteria, explore the determinants of innovativeness recognition, and discuss the implications of the 2025 revision for value assessment and market access.

methodsAll AIFA innovativeness reports available up to June 2025 were systematically reviewed and coded across the three appraisal domains - therapeutic need, added therapeutic value, and quality of evidence - together with contextual and regulatory variables (orphan designation, study design, EMA approval type, accelerated assessment, and PRIME designation). Descriptive and multinomial regression analysis were performed to identify predictors of appraisal outcomes and to explore associations with European and national timelines.

resultsAmong 294 appraisals, 27% were fully innovative, 29% conditionally innovative, and 44% non-innovative. ATV and quality of evidence were the strongest determinants, while therapeutic need played a secondary role. Orphan designation, pediatric/mixed populations, and the availability of RCT-based evidence increased the likelihood of a positive outcome. Medicines with EMA accelerated assessment were more often granted full innovativeness but did not achieve shorter national reimbursement timelines (median 432 days). Fully innovative medicines followed shorter EMA pathways (median 330 vs. 448 days), though not necessarily implying faster national access.

conclusionsAIFA's framework proved internal coherence, with ATV as the main driver. The 2025 criteria may enhance methodological rigor but reduce flexibility, requiring continuous monitoring to ensure timely and equitable access.

Indexed as

Added therapeutic valueAIFA (italian medicines agency)Drug innovativenessHealth technology assessment (HTA)Market accessRegulatory timelines

Identifiers

PMID42479353

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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.