Aloudah Nouf M, Shaman Ahmed M
Department of Clinical Pharmacy, College of Pharmacy, King Saud University, Riyadh 11523, Saudi Arabia.
Pharmacy (Basel). 2024 Nov 12;12(6):167. doi: 10.3390/pharmacy12060167.
Clinical trials conducted by pharmaceutical companies are essential for bridging local research efforts with broader populations, facilitating the transfer of valuable insights and solutions. This study aimed to explore the barriers and facilitators affecting clinical trials in Saudi Arabia from the perspective of key personnel within the pharmaceutical industry and Contract Research Organizations (CROs). We conducted in-depth semi-structured interviews with nine participants, which provided a holistic understanding of the intricate dynamics shaping the landscape of clinical trials in the country. The analysis revealed three prominent themes: operational challenges, complexities in navigating approval hurdles, and the unique value proposition for conducting clinical trials in Saudi Arabia. The participants expressed pride in the local infrastructure but acknowledged existing flaws, particularly in regulatory processes that contribute to delays in trial initiation. They emphasized the importance of conducting clinical trials in areas such as diabetes, crowd management during pilgrimages, and rare diseases, which are prevalent in the region. Despite the limited number of clinical trials registered (354 from 2009 to 2020, with only 1% being phase 1 studies), Saudi Arabia's total pharmaceutical market exceeds SAR 13 billion, positioning it as the largest market in the region. Stakeholders recognized the country's potential as a research hub, particularly within the Gulf Cooperative Council (GCC) region. However, to attract more trials and enhance the medical research landscape, it is crucial to address the identified barriers, streamline processes, and improve stakeholder alignment. The findings highlight the need for targeted interventions to overcome these challenges and leverage Saudi Arabia's investments in healthcare infrastructure since its transformation program launched in 2010. By enhancing the regulatory environment and fostering collaboration among stakeholders, Saudi Arabia can solidify its role as a key player in international clinical research.
制药公司开展的临床试验对于将本地研究工作与更广泛人群联系起来、促进宝贵见解和解决方案的传播至关重要。本研究旨在从制药行业和合同研究组织(CRO)的关键人员角度,探讨影响沙特阿拉伯临床试验的障碍和促进因素。我们对九名参与者进行了深入的半结构化访谈,从而全面了解塑造该国临床试验格局的复杂动态。分析揭示了三个突出主题:运营挑战、审批障碍的复杂性以及在沙特阿拉伯开展临床试验的独特价值主张。参与者对当地基础设施表示自豪,但也承认存在缺陷,特别是在导致试验启动延迟的监管流程方面。他们强调在糖尿病、朝圣期间的人群管理以及该地区普遍存在的罕见疾病等领域开展临床试验的重要性。尽管注册的临床试验数量有限(2009年至2020年为354项,其中只有1%为一期研究),但沙特阿拉伯的药品总市场超过130亿沙特里亚尔,使其成为该地区最大的市场。利益相关者认识到该国作为研究中心的潜力,特别是在海湾合作委员会(GCC)地区。然而,为了吸引更多试验并改善医学研究格局,解决已确定的障碍、简化流程并改善利益相关者的协调至关重要。研究结果凸显了采取针对性干预措施以克服这些挑战并利用沙特阿拉伯自2010年启动转型计划以来在医疗基础设施方面的投资的必要性。通过改善监管环境并促进利益相关者之间的合作,沙特阿拉伯可以巩固其在国际临床研究中的关键角色。