Gao Huaye, Li Jintong, Chen Xiaoping, Sun Zhanguo, Cui Gang, Cheng Minlu, Ding Li
Department of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Drug Clinical Trial Research Center, China-Japan Friendship Hospital, Beijing, China.
Front Pharmacol. 2022 Dec 15;13:1064364. doi: 10.3389/fphar.2022.1064364. eCollection 2022.
101BHG-D01 is a novel, long-acting, selective muscarinic receptor antagonist for the treatment of chronic obstructive pulmonary disease (COPD). A single-site, randomized, double-blind, placebo-controlled and dose-escalation study of 101BHG-D01 inhalation aerosol was conducted to evaluate its pharmacokinetics, metabolite profiling, safety and tolerability following the single inhaled doses ranged from 20 to 900 μg in healthy Chinese subjects. After inhalation, 101BHG-D01 was absorbed rapidly into plasma with the time to maximum concentration about 5 min, and eliminated slowly with the terminal phase half-life about 30 h. The cumulative excretion rates of 101BHG-D01 in feces and urine were about 30% and 2%, respectively, which showed the study drug was mainly excreted in feces. The maximum drug concentration and area under the plasma concentration-time curve increased with dose escalation in the range of 20-600 μg, but their values increased out of proportion to the whole studied doses. The main metabolic pathways were loss of phenyl group and hydroxylation. No metabolite that presented at greater than 10 percent of total drug-related exposure was observed. 101BHG-D01 was safe and well tolerated after administration. The study results indicate that 101BHG-D01 is a good candidate for the treatment of COPD and enable further clinical development in subsequent studies in patients. http://www.chinadrugtrials.org.cn; Identifier: CTR20192058.
101BHG-D01是一种新型长效选择性毒蕈碱受体拮抗剂,用于治疗慢性阻塞性肺疾病(COPD)。开展了一项关于101BHG-D01吸入气雾剂的单中心、随机、双盲、安慰剂对照及剂量递增研究,以评估健康中国受试者单次吸入20至900μg剂量后其药代动力学、代谢物谱、安全性和耐受性。吸入后,101BHG-D01迅速吸收入血浆,达峰时间约为5分钟,消除缓慢,终末相半衰期约为30小时。101BHG-D01在粪便和尿液中的累积排泄率分别约为30%和2%,表明研究药物主要经粪便排泄。在20 - 600μg范围内,最大药物浓度和血浆浓度-时间曲线下面积随剂量递增而增加,但其值的增加与整个研究剂量不成比例。主要代谢途径为苯基丢失和羟基化。未观察到占总药物相关暴露量超过10%的代谢物。给药后101BHG-D01安全且耐受性良好。研究结果表明,101BHG-D01是治疗COPD的良好候选药物,可在后续患者研究中进一步开展临床研发。 http://www.chinadrugtrials.org.cn; 标识符:CTR20192058