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全球控制和消除疟疾的新药研发管道。

The global pipeline of new medicines for the control and elimination of malaria.

机构信息

Medicines for Malaria Venture (MMV), 20 rte de Pré-Bois 1215, Geneva, Switzerland.

出版信息

Malar J. 2012 Sep 7;11:316. doi: 10.1186/1475-2875-11-316.

Abstract

Over the past decade, there has been a transformation in the portfolio of medicines to combat malaria. New fixed-dose artemisinin combination therapy is available, with four different types having received approval from Stringent Regulatory Authorities or the World Health Organization (WHO). However, there is still scope for improvement. The Malaria Eradication Research agenda identified several gaps in the current portfolio. Simpler regimens, such as a single-dose cure are needed, compared with the current three-day treatment. In addition, new medicines that prevent transmission and also relapse are needed, but with better safety profiles than current medicines. There is also a big opportunity for new medicines to prevent reinfection and to provide chemoprotection. This study reviews the global portfolio of new medicines in development against malaria, as of the summer of 2012. Cell-based phenotypic screening, and 'fast followers' of clinically validated classes, mean that there are now many new classes of molecules starting in clinical development, especially for the blood stages of malaria. There remain significant gaps for medicines blocking transmission, preventing relapse, and long-duration molecules for chemoprotection. The nascent pipeline of new medicines is significantly stronger than five years ago. However, there are still risks ahead in clinical development and sustainable funding of clinical studies is vital if this early promise is going to be delivered.

摘要

在过去的十年中,抗疟疾药物的种类发生了转变。新的固定剂量青蒿素复方疗法已经问世,其中有四种不同类型的药物已经获得了严格监管机构或世界卫生组织(WHO)的批准。但是,仍有改进的空间。消灭疟疾研究议程确定了当前药物组合中的几个空白。与目前的三天疗程相比,需要更简单的方案,如单剂量治疗。此外,还需要新的预防传播和复发的药物,但安全性要优于现有药物。新的药物也有很大的机会用于预防再感染和提供化学保护。本研究回顾了截至 2012 年夏季全球开发的抗疟疾新药组合。基于细胞的表型筛选和经过临床验证的药物的“快速跟进者”意味着,现在有许多新的分子类别开始进入临床开发阶段,特别是针对疟疾的血液阶段。在阻断传播、预防复发以及长效化学保护方面的药物仍然存在显著差距。新药物的新兴管道比五年前明显增强。然而,在临床开发中仍存在风险,可持续的临床研究资金对于实现这一早期承诺至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95ec/3472257/2a5088d6f439/1475-2875-11-316-1.jpg

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