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缩短成人和儿科药物制剂之间长达十年的差距:基于中低收入国家艾滋病毒经验的新框架。

Shortening the decade-long gap between adult and paediatric drug formulations: a new framework based on the HIV experience in low- and middle-income countries.

机构信息

World Health Organization, Geneva, Switzerland.

Clinton Health Access Initiative, Boston, MA, USA.

出版信息

J Int AIDS Soc. 2018 Feb;21 Suppl 1(Suppl Suppl 1). doi: 10.1002/jia2.25049.

Abstract

INTRODUCTION

Despite the coordinated efforts by several stakeholders to speed up access to HIV treatment for children, development of optimal paediatric formulations still lags 8 to 10 years behind that of adults, due mainly to lack of market incentives and technical complexities in manufacturing. The small and fragmented paediatric market also hinders launch and uptake of new formulations. Moreover, the problems affecting HIV similarly affect other disease areas where development and introduction of optimal paediatric formulations is even slower. Therefore, accelerating processes for developing and commercializing optimal paediatric drug formulations for HIV and other disease areas is urgently needed.

DISCUSSION

The Global Accelerator for Paediatric Formulations (GAP-f) is an innovative collaborative model that will accelerate availability of optimized treatment options for infectious diseases, such as HIV, tuberculosis and viral hepatitis, affecting children in low- and middle-income countries (LMICs). It builds on the HIV experience and existing efforts in paediatric drug development, formalizing collaboration between normative bodies, research networks, regulatory agencies, industry, supply and procurement organizations and funding bodies. Upstream, the GAP-f will coordinate technical support to companies to design and study optimal paediatric formulations, harmonize efforts with regulators and incentivize manufacturers to conduct formulation development. Downstream, the GAP-f will reinforce coordinated procurement and communication with suppliers. The GAP-f will be implemented in a three-stage process: (1) development of a strategic framework and promotion of key regulatory efficiencies; (2) testing of feasibility and results, building on the work of existing platforms such as the Paediatric HIV Treatment Initiative (PHTI) including innovative approaches to incentivize generic development and (3) launch as a fully functioning structure.

CONCLUSIONS

GAP-f is a key partnership example enhancing North-South and international cooperation on and access to science and technology and capacity building, responding to Sustainable Development Goal (SDG) 17.6 (technology) and 17.9. (capacity-building). By promoting access to the most needed paediatric formulations for HIV and high-burden infectious diseases in low-and middle-income countries, GAP-f will support achievement of SDG 3.2 (infant mortality), 3.3 (end of AIDS and combat other communicable diseases) and 3.8 (access to essential medicines), and be an essential component of meeting the global Start Free, Stay Free, AIDS Free super-fast-track targets.

摘要

简介

尽管有几个利益相关者协调努力加快为儿童提供艾滋病毒治疗,但由于缺乏市场激励和制造技术的复杂性,儿科配方的最佳开发仍落后成人 8 到 10 年。儿科市场规模较小且分散,也阻碍了新配方的推出和采用。此外,影响艾滋病毒的问题同样影响到其他疾病领域,这些领域开发和引入最佳儿科配方的速度更慢。因此,迫切需要加快为艾滋病毒和其他疾病领域开发和商业化最佳儿科药物配方的进程。

讨论

全球儿科配方加速基金(GAP-f)是一种创新的合作模式,将加速为受艾滋病毒、结核病和病毒性肝炎等传染病影响的中低收入国家的儿童提供优化的治疗选择。它以艾滋病毒的经验和现有的儿科药物开发工作为基础,使规范机构、研究网络、监管机构、行业、供应和采购组织以及供资机构之间的合作正式化。在前期,GAP-f 将协调向公司提供技术支持,以设计和研究最佳儿科配方,与监管机构协调努力,并激励制造商进行配方开发。在下游,GAP-f 将加强与供应商的协调采购和沟通。GAP-f 将分三个阶段实施:(1)制定战略框架和促进关键监管效率;(2)测试可行性和结果,利用现有的平台,如儿科艾滋病毒治疗倡议(PHTI),包括激励通用开发的创新方法;(3)作为一个功能齐全的结构推出。

结论

GAP-f 是加强南北合作和国际合作以及获取科学技术和能力建设的一个重要伙伴关系范例,符合可持续发展目标 17.6(技术)和 17.9(能力建设)。通过促进中低收入国家最需要的艾滋病毒和高负担传染病的儿科配方的获取,GAP-f 将支持实现可持续发展目标 3.2(婴儿死亡率)、3.3(结束艾滋病和防治其他传染病)和 3.8(获取基本药物),并成为实现全球快速启动、持续免费、艾滋病自由超级快车道目标的重要组成部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55ab/5978668/4bfafd6b2910/JIA2-21-e25049-g001.jpg

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