ClinOpsHub s.r.l., 72023 Mesagne, Italy.
Department of Biological and Environmental Science and Technologies (Di.S.Te.B.A.), University of Salento, 73100 Lecce, Italy.
Int J Environ Res Public Health. 2022 Oct 28;19(21):14023. doi: 10.3390/ijerph192114023.
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.
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.
一期临床试验是药物开发的关键阶段,因为新的候选治疗药物首次在人体上进行测试。 因此,为了减轻和控制对人类健康的潜在风险,国际准则和地方法律已经发布,这些准则和法律与赫尔辛基宣言和国际良好临床实践原则一致。 尽管有许多科学著作描述了 ClinicalTrials.gov 上注册的临床试验,但在欧洲,尚未研究一期临床试验的主要特征和趋势。 本研究旨在评估在五个最大的欧洲国家(2012-2021 年)进行的为期十年的一期临床试验的特征和分布趋势,并评估意大利监管框架对激活此类研究的影响。
对 ClinicalTrials.gov 数据库中注册的一期临床试验的主要数据和特征进行了调查,并随后进行了比较。 选择上述国家是基于官方政府网站上提供的人口统计学和国内生产总值(GDP)数据的相似性。
在分析的十年中,ClinicalTrials.gov 数据库中为这五个选定国家共登记了 6878 项一期临床试验; 这些研究主要是随机的(39.33%)和营利性的(76.64%)。 调查的最主要领域是肿瘤学(52.15%),其次是血液学(24.99%)和免疫学(12.04%)。 分析国家之间的差异表明,英国、德国和法国的一期临床试验数量减少最多,而西班牙和意大利则呈现稳定/增加趋势,尽管在 ClinicalTrials.gov 数据库中登记的试验数量较少。
意大利的注册一期临床试验数量最少,尽管多年来呈稳定趋势。 在这方面,意大利的监管框架必须紧急适应其他欧洲国家(西班牙是第一个实施新法规(欧盟)第 536/2014 号的国家),并简化临床试验申请程序,以提高该国的吸引力。 此外,应通过机构促进和支持非营利性一期临床试验(占意大利注册的一期临床试验总数的 19.81%,而盈利性一期临床试验为 80.19%),甚至从财务角度来看,以允许独立研究人员开发新的治疗药物。