HIV Department, World Health Organization, Geneva, Switzerland.
Division of AIDS, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
Clin Infect Dis. 2017 Jun 1;64(11):1597-1603. doi: 10.1093/cid/cix194.
Globally 1.8 million children are living with human immunodeficiency virus (HIV), yet only 51% of those eligible actually start treatment. Research and development (R&D) for pediatric antiretrovirals (ARVs) is a lengthy process and lags considerably behind drug development in adults. Providing safe, effective, and well-tolerated drugs for children remains critical to ensuring scale-up globally. We review current approaches to R&D for pediatric ARVs and suggest innovations to enable simplified, faster, and more comprehensive strategies to develop optimal formulations. Several approaches could be adopted, including focusing on a limited number of prioritized formulations and strengthening existing partnerships to ensure that pediatric investigation plans are developed early in the drug development process. Simplified and more efficient mechanisms to undertake R&D need to be put in place, and financing mechanisms must be made more sustainable. Lessons learned from HIV should be shared to support progress in developing pediatric formulations for other diseases, including tuberculosis and viral hepatitis.
全球有 180 万儿童感染了人类免疫缺陷病毒(HIV),但仅有 51%符合条件的儿童实际开始接受治疗。儿科抗逆转录病毒药物(ARV)的研发(R&D)是一个漫长的过程,远远落后于成人药物的开发。为儿童提供安全、有效且耐受性良好的药物对于确保全球范围内的扩大规模仍然至关重要。我们回顾了儿科 ARV 研发的当前方法,并提出了创新建议,以实现简化、更快和更全面的策略,开发最佳制剂。可以采用几种方法,包括专注于有限数量的优先制剂,并加强现有伙伴关系,以确保在药物开发过程的早期制定儿科研究计划。需要建立简化和更有效的研发机制,并且必须使融资机制更具可持续性。应分享从 HIV 中吸取的经验教训,以支持为其他疾病(包括结核病和病毒性肝炎)开发儿科制剂的进展。