Wells Timothy N C
Medicines for Malaria Venture, ICC, Block G, 3rd Floor, 20 Rue de Pre-Bois, PO Box 1826, 1215 Geneva 15, Switzerland.
Infect Disord Drug Targets. 2013 Aug;13(4):292-302. doi: 10.2174/1871526513666131129160156.
A steady increase in the number of antimalarial drug candidates since 2007 follows a call to eradicate malaria from the World Health Organization (WHO), the Bill and Melinda Gates Foundation and others. Four new fixed dose combination medicines have been approved by stringent authorities or the WHO in as many years. OZ439, a synthetic endoperoxide currently in Phase II, could reduce treatment to a single dose. Significant challenges remain: while drugs to treat patients suffering from malaria are essential, drugs focused on breaking the lifecycle between human and mosquito host are needed. Effective medicines that are easy to take in the field are needed, together with treatments for infants and for women in the first trimester of pregnancy. Research has concentrated on Plasmodium falciparum infection but there is a need for medicines that prevent relapses of P. vivax infection. In addition, the evolution of pathogen resistance against established drugs poses a threat to existing medicines. Direct testing of compounds against whole parasites as well as target approaches has accelerated the process of drug discovery, and identified new classes of compounds. The most advanced of these, spiroindolone, already in clinical development, kills the blood stages of both P. falciparum and P. vivax by a mechanism unrelated to any current antimalarial. The collaborative model of drug discovery between the Medicines for Malaria Venture, pharmaceutical companies and academic institutions has resulted in the construction of a promising pipeline of new classes of compounds, focused on the needs of the patient.
自2007年以来,抗疟候选药物的数量稳步增加,这是响应世界卫生组织(WHO)、比尔及梅琳达·盖茨基金会等机构根除疟疾的号召。多年来,已有四种新型固定剂量复方药物获得了严格监管当局或WHO的批准。OZ439是一种目前处于II期试验阶段的合成过氧化物,它有望将治疗简化为单次给药。然而,仍存在重大挑战:虽然治疗疟疾患者的药物至关重要,但还需要专注于打破人类与蚊子宿主之间生命周期的药物。需要易于在现场服用的有效药物,以及针对婴儿和怀孕头三个月妇女的治疗方法。研究主要集中在恶性疟原虫感染上,但也需要预防间日疟原虫感染复发的药物。此外,病原体对现有药物的耐药性演变对现有药物构成了威胁。针对全寄生虫的化合物直接测试以及靶向方法加速了药物发现过程,并确定了新的化合物类别。其中最先进的是已经进入临床开发阶段的螺环吲哚酮,它通过一种与任何现有抗疟药物无关的机制杀死恶性疟原虫和间日疟原虫的血液阶段。疟疾药物事业(Medicines for Malaria Venture)、制药公司和学术机构之间的药物发现合作模式,已经构建了一个有前景的新型化合物研发通道,专注于满足患者需求。