Trends of Phase I Clinical Trials in the Latest Ten Years across Five European Countries
Davide Di Tonno (),
Caterina Perlin,
Anna Chiara Loiacono,
Luca Giordano,
Laura Martena,
Stefano Lagravinese,
Federica Rossi,
Santo Marsigliante,
Michele Maffia,
Andrea Falco,
Prisco Piscitelli,
Alessandro Miani,
Susanna Esposito,
Alessandro Distante and
Alberto Argentiero
Additional contact information
Davide Di Tonno: ClinOpsHub s.r.l., 72023 Mesagne, Italy
Caterina Perlin: ClinOpsHub s.r.l., 72023 Mesagne, Italy
Anna Chiara Loiacono: ClinOpsHub s.r.l., 72023 Mesagne, Italy
Luca Giordano: ClinOpsHub s.r.l., 72023 Mesagne, Italy
Laura Martena: ClinOpsHub s.r.l., 72023 Mesagne, Italy
Stefano Lagravinese: ClinOpsHub s.r.l., 72023 Mesagne, Italy
Federica Rossi: ClinOpsHub s.r.l., 72023 Mesagne, Italy
Santo Marsigliante: Department of Biological and Environmental Science and Technologies (Di.S.Te.B.A.), University of Salento, 73100 Lecce, Italy
Michele Maffia: Department of Biological and Environmental Science and Technologies (Di.S.Te.B.A.), University of Salento, 73100 Lecce, Italy
Andrea Falco: Department of Public Health, European University of Madrid, 28670 Madrid, Spain
Prisco Piscitelli: Department of Biological and Environmental Science and Technologies (Di.S.Te.B.A.), University of Salento, 73100 Lecce, Italy
Alessandro Miani: Department of Environmental Science and Policy, University of Milan, 10123 Milan, Italy
Susanna Esposito: Pediatric Clinic, Department of Medicine and Surgery, University of Parma, 43121 Parma, Italy
Alessandro Distante: Euro Mediterranean Scientific Biomedical Institute (ISBEM), 72023 Mesagne, Italy
Alberto Argentiero: Department of Biological and Environmental Science and Technologies (Di.S.Te.B.A.), University of Salento, 73100 Lecce, Italy
IJERPH, 2022, vol. 19, issue 21, 1-10
Abstract:
Background: Phase 1 clinical trials represent a critical phase of drug development because new candidate therapeutic agents are tested for the first time on humans. Therefore, international guidelines and local laws have been released to mitigate and control possible risks for human health in agreement with the declaration of Helsinki and the international Good Clinical Practice principles. Despite numerous scientific works characterizing the registered clinical trials on ClinicalTrials.gov, the main features and trends of registered phase 1 clinical trials in Europe have not been investigated. This study is aimed at assessing the features and the temporal trend of distribution of phase 1 clinical studies, carried out in the five largest European countries over a ten-year period (2012–2021), and to evaluate the impact of the Italian regulatory framework on the activation of such studies. Methods: The main data and characteristics of phase 1 clinical studies registered on the ClinicalTrials.gov database for France, Germany, Italy, Spain and the United Kingdom have been investigated and subsequently compared. The above-mentioned countries were selected based on similarities in terms of demographic and Gross Domestic Product (GDP) data available on official government websites. (3) Results: A total number of 6878 phase 1 clinical trials were registered for the five selected countries in the ClinicalTrials.gov database during the ten years analyzed; the studies were predominantly randomized (39.33%) and for-profit (76.64%). The most represented area of investigations was oncology (52.15%), followed by hematology (24.99%) and immunology (12.04%). The variability observed between the analyzed countries showed that the UK, Germany and France presented the highest reduction in the number of phase 1 clinical trials, while for Spain and Italy, a stable/increased trend was observed, although with a lower number of trials registered on the ClinicalTrials.gov database. (4) Conclusions: Italy displayed the lowest number of registered phase 1 clinical trials, even though it showed a stable trend over the years. In this regard, the Italian regulatory framework must urgently be adapted to that of other European countries (Spain has been the first country to implement the new Regulation (EU) No 536/2014) and streamline the process of clinical trial application to increase the attractiveness of the country. Moreover, nonprofit phase 1 clinical trials (which represent 19.81% of the total number of phase 1 clinical trials registered in Italy vs. 80.19% of profit phase 1 clinical studies) should be promoted and supported by the institutions, even from a financial point of view, to allow independent researchers to develop new therapeutic drugs.
Keywords: phase 1 clinical trials; Europe; trends; ClinicalTrials.gov database (search for similar items in EconPapers)
JEL-codes: I I1 I3 Q Q5 (search for similar items in EconPapers)
Date: 2022
References: View complete reference list from CitEc
Citations:
Downloads: (external link)
https://www.mdpi.com/1660-4601/19/21/14023/pdf (application/pdf)
https://www.mdpi.com/1660-4601/19/21/14023/ (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:gam:jijerp:v:19:y:2022:i:21:p:14023-:d:955663
Access Statistics for this article
IJERPH is currently edited by Ms. Jenna Liu
More articles in IJERPH from MDPI
Bibliographic data for series maintained by MDPI Indexing Manager ().