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Trends of Phase I Clinical Trials in the Latest Ten Years across Five European Countries
Davide Di Tonno1,2, Caterina Perlin1,2, Anna Chiara Loiacono1,2
1ClinOpsHub s.r.l., 72023 Mesagne, Italy.
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.
Insights
Phase 1 clinical trials in Europe are predominantly for-profit oncology studies. While the UK, Germany, and France saw decreases, Spain and Italy maintained stable trends, highlighting Italy
Area of Science:
- Drug Development
- Clinical Research
- Oncology
Background:
- Phase 1 clinical trials are crucial for testing new therapeutic agents in humans.
- International guidelines and local laws govern these trials to ensure patient safety.
- Previous studies have characterized clinical trials, but European Phase 1 trends remain under-investigated.
Purpose of the Study:
- To assess the features and temporal trends of Phase 1 clinical studies in five major European countries (France, Germany, Italy, Spain, UK) from 2012-2021.
- To evaluate the impact of the Italian regulatory framework on Phase 1 trial activation.
- To compare Phase 1 clinical trial data across selected European nations.
Main Methods:
- Analysis of Phase 1 clinical studies registered on ClinicalTrials.gov for France, Germany, Italy, Spain, and the UK between 2012 and 2021.
- Countries were selected based on demographic and GDP similarities.
- Data investigated included study characteristics, trends, and regulatory impact.
Main Results:
- A total of 6878 Phase 1 clinical trials were registered across the five countries.
- The majority of trials were randomized (39.33%) and for-profit (76.64%).
- Oncology dominated investigations (52.15%), followed by hematology (24.99%) and immunology (12.04%).
- The UK, Germany, and France showed the highest reduction in trials, while Spain and Italy exhibited stable or increasing trends.
- Italy registered the lowest number of trials despite a stable trend.
Conclusions:
- Italy's regulatory framework needs adaptation to match other European countries and streamline clinical trial applications.
- Promoting and supporting non-profit Phase 1 trials in Italy is essential for independent drug development.
- Regulatory harmonization is needed to enhance Italy's attractiveness for clinical research.
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