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新型磷脂酰肌醇 4-激酶抑制剂 MMV390048 在健康志愿者中的安全性、耐受性、药代动力学和抗疟活性。

Safety, Tolerability, Pharmacokinetics, and Antimalarial Activity of the Novel Phosphatidylinositol 4-Kinase Inhibitor MMV390048 in Healthy Volunteers.

机构信息

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

UCT MRC Collaborating Centre for Optimising Antimalarial Therapy, University of Cape Town, Cape Town, South Africa.

出版信息

Antimicrob Agents Chemother. 2020 Mar 24;64(4). doi: 10.1128/AAC.01896-19.

Abstract

MMV390048 is a novel antimalarial compound that inhibits phosphatidylinositol-4-kinase. The safety, tolerability, pharmacokinetic profile, and antimalarial activity of MMV390048 were determined in healthy volunteers in three separate studies. A first-in-human, double-blind, randomized, placebo-controlled, single-ascending-dose study was performed. Additionally, a volunteer infection study investigated the antimalarial activity of MMV390048 using the induced blood-stage malaria (IBSM) model. Due to the high pharmacokinetic variability with the powder-in-bottle formulation used in both of these studies, a third study was undertaken to select a tablet formulation of MMV390048 to take forward into future studies. MMV390048 was generally well tolerated when administered as a single oral dose up to 120 mg, with rapid absorption and a long elimination half-life. Twelve adverse events were considered to be potentially related to MMV390048 in the first-in-human study but with no obvious correlation between these and MMV390048 dose or exposure. Although antimalarial activity was evident in the IBSM study, rapid recrudescence occurred in most subjects after treatment with 20 mg MMV390048, a dose expected to be subtherapeutic. Reformulation of MMV390048 into two tablet formulations (tartaric acid and Syloid) resulted in significantly reduced intersubject pharmacokinetic variability. Overall, the results of this study suggest that MMV390048 is well tolerated in humans, and the pharmacokinetic properties of the compound indicate that it has the potential to be used for antimalarial prophylaxis or inclusion in a single-dose cure. MMV390048 is currently being tested in a phase 2a study in Ethiopian adults with acute, uncomplicated falciparum or vivax malaria monoinfection. (The three clinical trials described here were each registered with ClinicalTrials.gov as follows: first-in-human study, registration no. NCT02230579; IBSM study, registration no. NCT02281344; and formulation optimization study, registration no. NCT02554799.).

摘要

MMV390048 是一种新型抗疟化合物,可抑制磷脂酰肌醇-4-激酶。在三项独立研究中,在健康志愿者中确定了 MMV390048 的安全性、耐受性、药代动力学特征和抗疟活性。进行了首次人体、双盲、随机、安慰剂对照、单次递增剂量研究。此外,一项志愿者感染研究使用诱导的血期疟疾(IBSM)模型研究了 MMV390048 的抗疟活性。由于在这两项研究中使用的瓶装粉末制剂存在高药代动力学变异性,因此进行了第三项研究以选择 MMV390048 的片剂制剂推进到未来的研究中。当作为单次口服剂量高达 120mg 给药时,MMV390048 通常具有良好的耐受性,具有快速吸收和长消除半衰期。在首次人体研究中,有 12 种不良事件被认为与 MMV390048 可能相关,但这些不良事件与 MMV390048 剂量或暴露之间没有明显的相关性。虽然在 IBSM 研究中观察到抗疟活性,但在用 20mg MMV390048 治疗后,大多数受试者中迅速复发,这一剂量预计是治疗性的。将 MMV390048 重新配方为两种片剂制剂(酒石酸和 Syloid)导致受试者间药代动力学变异性显著降低。总的来说,这项研究的结果表明,MMV390048 在人体中耐受良好,化合物的药代动力学特性表明它有可能用于抗疟预防或纳入单剂量治疗。MMV390048 目前正在埃塞俄比亚患有急性、无并发症的恶性疟原虫或间日疟原虫单一感染的成年人中进行 2a 期研究。(这里描述的三项临床试验均在 ClinicalTrials.gov 上注册如下:首次人体研究,注册号 NCT02230579;IBSM 研究,注册号 NCT02281344;和制剂优化研究,注册号 NCT02554799。)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f60/7179259/eff03d40dad0/AAC.01896-19-f0001.jpg

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