Phase I Clinical Trial Unit, First Hospital, Jilin University, Changchun, China.
Department of Clinical Laboratory, First Hospital, Jilin University, Changchun, China.
Antimicrob Agents Chemother. 2022 May 17;66(5):e0009422. doi: 10.1128/aac.00094-22. Epub 2022 Apr 11.
GST-HG131, a novel dihydroquinolizinone (DHQ) compound, has been shown to reduce circulating levels of HBsAg in animals. This first-in-human trial evaluated the safety, tolerability, and pharmacokinetic profile of GST-HG131 in healthy Chinese subjects. This was a double-blind, randomized, placebo-controlled phase Ia clinical trial that was conducted in two parts. Part A was a single-ascending-dose (SAD; GST-HG131 10 30, 60, 100, 150, 200, 250 or 300 mg or placebo) study, which also assessed the food effect of GST-HG131 100 mg. Part B was a multiple-ascending-dose (MAD; GST-HG131 30, 60 or 100 mg or placebo BID) study. Tolerability assessments included adverse events, vital signs, 12-lead electrocardiogram, physical examination, and clinical laboratory tests. PK analyses were conducted in blood, urine, and fecal samples. Single doses of GST-HG131 ≤ 300 mg and multiple doses of GST-HG131 ≤ 60 mg were generally safe and well tolerated; however, multiple dosing was stopped at GST-HG131 100 mg, as pre-defined stopping rules specified in the protocol were met (Grade II drug related AEs of nausea and dizziness in >50% of subjects). In the SAD study, median t of GST-HG131 was 1-6 h, and t ranged from 3.88 h to 14.3 h. PK parameters were proportional to dose. Exposure was reduced after food intake. In the MAD study, steady-state was attained on day 4, and there was no apparent plasma accumulation of GST-HG131 on day 7 (R < 1.5). In conclusion, GST-HG131 exhibited an acceptable safety profile in healthy subjects at single doses ranging from 10-300 mg and multiple doses (BID) ranging from 30-60 mg, and the MAD doses (30 mg and 60 mg BID) that potentially meet the therapeutic AUC requirements. These findings imply GST-HG131 has potential as a therapeutic option for CHB infection. (This study has been registered at ClinicalTrials.gov under identifier NCT04499443.).
GST-HG131 是一种新型的二氢喹啉酮 (DHQ) 化合物,已被证明可降低动物体内 HBsAg 的循环水平。这项首次在人体中进行的试验评估了 GST-HG131 在健康中国受试者中的安全性、耐受性和药代动力学特征。这是一项双盲、随机、安慰剂对照的 Ia 期临床试验,分为两部分进行。第 A 部分是单次递增剂量 (SAD;GST-HG131 10、30、60、100、150、200、250 或 300mg 或安慰剂) 研究,还评估了 GST-HG131 100mg 的饮食影响。第 B 部分是多次递增剂量 (MAD;GST-HG131 30、60 或 100mg 或安慰剂 BID) 研究。耐受性评估包括不良事件、生命体征、12 导联心电图、体格检查和临床实验室检查。PK 分析在血液、尿液和粪便样本中进行。单次剂量 GST-HG131≤300mg 和多次剂量 GST-HG131≤60mg 通常是安全且耐受良好的;然而,由于协议中规定的预定停药规则得到满足(恶心和头晕的药物相关不良事件发生率超过 50%),停止了多次给药剂量至 GST-HG131 100mg。在 SAD 研究中,GST-HG131 的中位数 t 为 1-6 小时,t 范围为 3.88 小时至 14.3 小时。PK 参数与剂量成正比。进食后暴露减少。在 MAD 研究中,第 4 天达到稳态,第 7 天 GST-HG131 无明显血浆蓄积(R<1.5)。总之,GST-HG131 在健康受试者中单剂量 10-300mg 和多剂量(BID)30-60mg 范围内表现出可接受的安全性特征,并且多剂量(30mg 和 60mg BID)可能满足治疗 AUC 要求。这些发现表明 GST-HG131 作为 CHB 感染的治疗选择具有潜力。(本研究已在 ClinicalTrials.gov 注册,标识符为 NCT04499443。)