1Medicines for Malaria Venture, Geneva, Switzerland.
2SGS Life Sciences, Antwerp, Belgium.
Am J Trop Med Hyg. 2021 Feb 8;104(4):1348-1358. doi: 10.4269/ajtmh.20-1165.
P218 is a highly selective dihydrofolate reductase inhibitor with potent in vitro activity against pyrimethamine-resistant Plasmodium falciparum. This single-center, randomized, double-blind, placebo-controlled phase Ib study evaluated P218 safety, pharmacokinetics, and chemoprotective efficacy in a P. falciparum sporozoite (PfSPZ) volunteer infection study (VIS). Consecutive dose safety and tolerability were evaluated (cohort 1), with participants receiving two oral doses of P218 1,000 mg 48 hours apart (n = 6), or placebo (n = 2). P218 chemoprotective efficacy was assessed (cohorts 2 and 3) with direct venous inoculation of 3,200 aseptic, cryopreserved PfSPZ (NF54 strain) followed 2 hours later with two P218 doses of 1,000 mg (cohort 2, n = 9) or 100 mg (cohort 3, n = 9) administered 48 hours apart, or placebo (n = 6). Parasitemia was assessed from day 7 using quantitative PCR targeting the var gene acidic terminal sequence (varATS qPCR). By day 28, all participants in cohort 2 (P218 1,000 mg) and 8/9 in cohort 3 (P218 100 mg) were sterilely protected post-PfSPZ VIS, confirming P218 P. falciparum chemoprotective activity. With placebo, all six participants became parasitemic (geometric mean time to positive parasitemia 10.6 days [90% CI: 9.9-11.4]). P218 pharmacokinetics were similar in participants with or without induced infection. Adverse events of any cause occurred in 45.8% (11/24) of participants who received P218 and 50.0% (4/8) following placebo; all were mild/moderate in severity, transient, and self-limiting. There were no clinically relevant changes in laboratory parameters, vital signs, or electrocardiograms. P218 displayed excellent chemoprotective efficacy against P. falciparum with favorable safety and tolerability.
P218 是一种高度选择性的二氢叶酸还原酶抑制剂,对耐乙胺嘧啶的恶性疟原虫具有强大的体外活性。这项单中心、随机、双盲、安慰剂对照的 1b 期研究评估了 P218 在恶性疟原虫孢子(PfSPZ)志愿者感染研究(VIS)中的安全性、药代动力学和化学保护功效。连续评估剂量安全性和耐受性(第 1 队列),参与者接受 2 次口服 P218 1000mg,间隔 48 小时(n=6)或安慰剂(n=2)。用 3200 个无菌冷冻 PfSPZ(NF54 株)直接静脉接种,2 小时后用 2 次 P218 剂量 1000mg(第 2 队列,n=9)或 100mg(第 3 队列,n=9),间隔 48 小时给予 P218 或安慰剂(n=6)。从第 7 天开始,使用针对 var 基因酸性末端序列(varATS qPCR)的定量 PCR 评估寄生虫血症。到第 28 天,第 2 队列(P218 1000mg)中的所有参与者和第 3 队列(P218 100mg)中的 8/9 名参与者在 PfSPZ VIS 后均无菌保护,证实了 P218 对恶性疟原虫的化学保护活性。用安慰剂,所有 6 名参与者均出现寄生虫血症(阳性寄生虫血症的几何平均时间为 10.6 天[90%CI:9.9-11.4])。有或没有诱导感染的参与者的 P218 药代动力学相似。接受 P218 的参与者中任何原因的不良事件发生率为 45.8%(11/24),安慰剂组为 50.0%(4/8);所有不良事件均为轻度/中度、短暂和自限性。实验室参数、生命体征或心电图无临床相关变化。P218 对恶性疟原虫具有极好的化学保护功效,且安全性和耐受性良好。