Kelly A S, Fox C K, Rudser K D, Gross A C, Ryder J R
Department of Pediatrics, University of Minnesota Medical School, and University of Minnesota Masonic Children's Hospital, Minneapolis, MN, USA.
Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
Int J Obes (Lond). 2016 Jul;40(7):1043-50. doi: 10.1038/ijo.2016.69. Epub 2016 Apr 26.
Despite the increasing number of medications recently approved to treat obesity among adults, few agents have been formally evaluated in children or adolescents for this indication. Moreover, there is a paucity of guidance in the literature addressing best practices with regard to pediatric obesity pharmacotherapy clinical trial design, and only general recommendations have been offered by regulatory agencies on this topic. The purposes of this article are to (1) offer a background of the current state of the field of pediatric obesity medicine, (2) provide a brief review of the literature summarizing pediatric obesity pharmacotherapy clinical trials, and (3) highlight and discuss some of the unique aspects that should be considered when designing and conducting high-quality clinical trials evaluating the safety and efficacy of obesity medications in children and adolescents. Suggestions are offered in the areas of target population and eligibility criteria, clinical trial end-point selection, trial duration, implementation of lifestyle modification therapy and recruitment and retention of participants. Efforts should be made to design and conduct trials appropriately to ensure that high-quality evidence is generated on the safety and efficacy of various medications used to treat pediatric obesity.
尽管最近获批用于治疗成人肥胖症的药物数量不断增加,但很少有药物针对这一适应症在儿童或青少年中进行过正式评估。此外,文献中缺乏关于儿科肥胖药物治疗临床试验设计最佳实践的指导,监管机构在这个问题上也只提供了一般性建议。本文的目的是:(1)介绍儿科肥胖医学领域的现状背景;(2)简要回顾总结儿科肥胖药物治疗临床试验的文献;(3)强调并讨论在设计和开展评估肥胖药物在儿童和青少年中的安全性和有效性的高质量临床试验时应考虑的一些独特方面。在目标人群和入选标准、临床试验终点选择、试验持续时间、生活方式改变疗法的实施以及参与者的招募和留存等方面提出了建议。应努力进行适当的试验设计和实施,以确保获得关于用于治疗儿科肥胖的各种药物的安全性和有效性的高质量证据。