Abman Steven H, Nikkho Sylvia M, Berger Rolf M F, Del Cerro Maria Jesus, Austin Eric D, Beghetti Maurice, Ivy Dunbar, Griffiths Megan, Hilgendorff Anne, Kawut Steven H, Krishnan Usha S, Mullen Mary P, Moledina Shahin, Thébaud Bernard, Stockbridge Norman
Department of Paediatrics, Paediatric Heart Lung Center University of Colorado School of Medicine Aurora Colorado USA.
Clinical Development, Bayer AG Berlin Germany.
Pulm Circ. 2025 Jul 15;15(3):e70126. doi: 10.1002/pul2.70126. eCollection 2025 Jul.
As with adult pulmonary hypertension (PH), high morbidity and mortality persist with diverse types of paediatric PH. Despite major advances in pharmacologic therapies based on extensive studies in adult PH, few drugs have been comprehensively studied in neonates, infants, and children, leaving current paediatric PH care largely dependent on small observational studies and extrapolation of evidence from adult clinical trials. Challenges in developing successful clinical trials in children include the need to define distinct disease phenotypes with well-characterised natural history and outcomes, the lack of established age- and disease-specific study endpoints, small and heterogeneous paediatric populations, and the common off-label use of PH-targeted drug therapies without regulatory approval. From a regulatory perspective, sufficient studies of safety, pharmacokinetics, and pharmacodynamics in neonates and young children are often lacking, and the potential role for bridging biomarkers has been underexplored. Additional opportunities include developing innovative trial designs, employing real-world data from existing registries, and fostering collaborations among sponsors, regulatory authorities, physicians, patients, and their families. By reducing reliance on off-label drug use and leveraging paediatric PH registry data, this approach offers a path toward more effective and evidence-based treatment protocols for paediatric patients. This review provides an overview of integrated international perspectives from an interprofessional platform that includes academia, the pharmaceutical industry, and regulatory agencies surrounding the future design of clinical trials for paediatric PH. Ongoing evaluation and adaptation of these strategies will be essential for ensuring that paediatric PH patients receive the highest standard of care.
与成人肺动脉高压(PH)一样,各种类型的儿科PH的发病率和死亡率仍然很高。尽管基于成人PH的广泛研究,药物治疗取得了重大进展,但很少有药物在新生儿、婴儿和儿童中进行过全面研究,目前儿科PH的治疗在很大程度上依赖于小型观察性研究以及从成人临床试验中推断证据。在儿童中开展成功的临床试验面临的挑战包括需要定义具有明确自然病史和预后的不同疾病表型、缺乏既定的年龄和疾病特异性研究终点、儿科人群规模小且异质性大,以及在未经监管批准的情况下普遍超说明书使用针对PH的药物治疗。从监管角度来看,新生儿和幼儿的安全性、药代动力学和药效学的充分研究往往缺乏,而且桥接生物标志物的潜在作用尚未得到充分探索。其他机会包括开发创新的试验设计、利用现有登记处的真实世界数据,以及促进申办者、监管机构、医生、患者及其家属之间的合作。通过减少对超说明书用药的依赖并利用儿科PH登记数据,这种方法为制定更有效且基于证据的儿科患者治疗方案提供了一条途径。本综述概述了来自一个跨专业平台的综合国际观点,该平台包括学术界、制药行业和监管机构,围绕儿科PH临床试验的未来设计展开。持续评估和调整这些策略对于确保儿科PH患者获得最高标准的护理至关重要。