PKU Care Luzhong Hospital, Shandong, China.
Phaeno Therapeutics Co. Ltd, Hangzhou, China.
Clin Pharmacol Drug Dev. 2022 Dec;11(12):1467-1473. doi: 10.1002/cpdd.1138. Epub 2022 Jul 6.
HN0037 is a helicase-primase inhibitor developed to treat herpes simplex virus (HSV) infection. This study evaluated the safety, tolerability, and pharmacokinetics of HN0037, following oral administration in healthy volunteers. This double-blind, placebo-controlled, phase 1 study comprised two parts. In part 1, a single escalating dose of 10, 30, 60, 120, 200, 300, and 400 mg was assessed, and the food effect was evaluated in the 200-mg cohort. In part 2, a multiple dose evaluation involving 30 and 100 mg once a day was conducted for 14 days. Following single oral doses, the systemic exposure of HN0037 increased in a proportional manner over the lower dose range (10-120 mg) and in a subproportional manner over the higher dose range (200-400 mg). Following multiple oral doses, significant drug accumulation of systemic exposure was found at steady state, and the half-life ranged 50.4-61.0 h. The food effect study results indicated that a high-fat meal had a marginal impact on HN0037's pharmacokinetics. No differences were observed in the incidence of adverse events between HN0037 and placebo groups in either study. These results demonstrate that HN0037 is safe and well-tolerated, supporting further clinical development.
HN0037 是一种开发用于治疗单纯疱疹病毒 (HSV) 感染的解旋酶-引物酶抑制剂。这项研究评估了健康志愿者口服 HN0037 的安全性、耐受性和药代动力学。这项双盲、安慰剂对照、I 期研究分为两部分。在第 1 部分中,评估了单剂量递增 10、30、60、120、200、300 和 400mg,并且在 200mg 队列中评估了食物效应。在第 2 部分中,进行了为期 14 天的 30 和 100mg 每日一次的多次剂量评估。单次口服给药后,HN0037 的全身暴露量在较低剂量范围内(10-120mg)呈比例增加,在较高剂量范围内(200-400mg)呈亚比例增加。多次口服给药后,在稳态时发现全身暴露量的药物蓄积显著,半衰期范围为 50.4-61.0h。食物效应研究结果表明,高脂肪餐对 HN0037 的药代动力学有轻微影响。在两项研究中,HN0037 组和安慰剂组不良事件的发生率均无差异。这些结果表明,HN0037 安全且耐受良好,支持进一步的临床开发。