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I 期和 II 期药物开发中抗疟药物候选物的范围审查。

Scoping Review of Antimalarial Drug Candidates in Phase I and II Drug Development.

机构信息

QIMR Berghofer Medical Research Institutegrid.1049.c, Brisbane, Queensland, Australia.

Biostatistics Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbournegrid.1008.9, Parkville, Victoria, Australia.

出版信息

Antimicrob Agents Chemother. 2022 Feb 15;66(2):e0165921. doi: 10.1128/AAC.01659-21. Epub 2021 Nov 29.

Abstract

The emergence and spread of parasite resistance to currently available antimalarials has highlighted the importance of developing novel antimalarials. This scoping review provides an overview of antimalarial drug candidates undergoing phase I and II studies between 1 January 2016 and 28 April 2021. PubMed, Web of Science, Embase, clinical trial registries, and reference lists were searched for relevant studies. Information regarding antimalarial compound details, clinical trial characteristics, study population, and drug pharmacokinetics and pharmacodynamics (PK-PD) were extracted. A total of 50 studies were included, of which 24 had published their results and 26 were unpublished. New antimalarial compounds were evaluated as monotherapy (28 studies, 14 drug candidates) and combination therapy (9 studies, 10 candidates). Fourteen active compounds were identified in the current antimalarial drug development pipeline together with 11 compounds that are inactive, 6 due to insufficient efficacy. PK-PD data were available from 24 studies published as open-access articles. Four unpublished studies have made their results publicly available on clinical trial registries. The terminal elimination half-life of new antimalarial compounds ranged from 14.7 to 483 h. The log parasite reduction ratio over 48 h and parasite clearance half-life for Plasmodium falciparum following a single-dose monotherapy were 1.55 to 4.1 and 3.4 to 9.4 h, respectively. The antimalarial drug development landscape has seen a number of novel compounds, with promising PK-PD properties, evaluated in phase I and II studies over the past 5 years. Timely public disclosure of PK-PD data is crucial for informative decision-making and drug development strategy.

摘要

寄生虫对现有抗疟药物的耐药性的出现和传播凸显了开发新抗疟药物的重要性。本范围综述概述了 2016 年 1 月 1 日至 2021 年 4 月 28 日期间正在进行 I 期和 II 期研究的抗疟药物候选物。检索了 PubMed、Web of Science、Embase、临床试验注册处和参考文献,以查找相关研究。提取了有关抗疟化合物详细信息、临床试验特征、研究人群以及药物药代动力学和药效学(PK-PD)的信息。共纳入 50 项研究,其中 24 项已发表结果,26 项为未发表。新的抗疟化合物被评估为单药治疗(28 项研究,14 种候选药物)和联合治疗(9 项研究,10 种候选药物)。在当前抗疟药物开发管道中确定了 14 种活性化合物,以及 11 种非活性化合物,其中 6 种由于疗效不足。24 项已发表的开放获取文章提供了 PK-PD 数据。四项未发表的研究已在临床试验注册处公开其结果。新抗疟化合物的终末消除半衰期范围为 14.7 至 483 小时。单次单药治疗后 48 小时内对数寄生虫减少率和疟原虫清除半衰期为 1.55 至 4.1 和 3.4 至 9.4 小时,分别。在过去 5 年中,I 期和 II 期研究评估了许多具有有前景的 PK-PD 特性的新型化合物,抗疟药物的开发领域出现了许多新型化合物,在过去 5 年中,I 期和 II 期研究评估了许多具有有前景的 PK-PD 特性的新型化合物。及时公开 PK-PD 数据对于信息决策和药物开发策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0479/8846400/63a30828fccd/aac.01659-21-f001.jpg

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