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101BHG-D01 鼻喷雾剂的安全性、耐受性和药代动力学研究,这是一种新型长效、选择性毒蕈碱型乙酰胆碱受体拮抗剂,在中国健康志愿者中的随机、双盲、安慰剂对照、单次递增、首次人体研究。

Safety, Tolerability, and Pharmacokinetic Study of 101BHG-D01 Nasal Spray, a Novel Long-Acting and Selective Cholinergic M Receptor Antagonist, in Healthy Chinese Volunteers: A Randomized, Double-Blind, Placebo-Controlled, Single-Dose Escalation, First-In-Human Study.

机构信息

Drug Clinical Trial Institution, Wuxi People's Hospital Affiliated with Nanjing Medical University, Wuxi, 214023, Jiangsu, China.

Beijing Shuobai Pharmaceutical Technology Co., Ltd., Beijing, China.

出版信息

Eur J Drug Metab Pharmacokinet. 2022 Jul;47(4):509-521. doi: 10.1007/s13318-022-00769-6. Epub 2022 Apr 16.

Abstract

BACKGROUND AND OBJECTIVE

101BHG-D01 nasal spray is the first novel long-acting cholinergic M receptor antagonist under development to treat rhinorrhea in rhinitis. This first-in-human study aimed to evaluate the safety, tolerability, and pharmacokinetics of 101BHG-D01 nasal spray following single intranasal doses in healthy Chinese subjects.

METHODS

A randomized, double-blind, placebo-controlled, single-dose escalation study was conducted in healthy Chinese volunteers after intranasal doses of 101BHG-D01 nasal spray or placebo ranging from 40 µg to 960 µg (total of six doses). Blood samples were collected at scheduled time points, and plasma concentrations were determined using a validated high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method. A non-compartmental method was used to calculate the main pharmacokinetic parameters, including the area under the plasma concentration-time curve from time zero to the time of the last measurable concentration (AUC), the area under the plasma concentration-time curve from time zero to infinity (AUC), the maximum plasma concentration (C), the time to maximum plasma concentration (T), and the elimination half-life (t). Safety was evaluated by monitoring adverse events, laboratory assays, vital signs, physical examinations, 12-lead electrocardiograms (ECGs), anterior rhinoscopy, ophthalmic examination, and ambulatory ECG monitoring.

RESULTS

Following single intranasal dosing, 101BHG-D01 was rapidly absorbed with a median T of 0.34-0.50 h and eliminated slowly with a mean t ranging from 4.29 to 46.76 h for different dose groups. The C and AUC of 101BHG-D01 increased linearly across the examined dose range of 40-960 µg. 101BHG-D01 nasal spray was well tolerated, all AEs were mild, and no serious adverse events occurred during the study.

CONCLUSIONS

101BHG-D01 nasal spray was safe and well tolerated in healthy Chinese subjects when administered intranasally in single escalating doses. The mean C and AUC increased proportionally to the studied dose. The pharmacokinetic, safety, and tolerability profiles of 101BHG-D01 nasal spray indicate that it is a good candidate for further development as a treatment for rhinorrhea in rhinitis.

摘要

背景和目的

101BHG-D01 鼻喷雾剂是首个正在开发用于治疗鼻炎鼻漏的新型长效胆碱能 M 受体拮抗剂。这项首次人体研究旨在评估健康中国受试者单次鼻内给予 101BHG-D01 鼻喷雾剂或安慰剂后的安全性、耐受性和药代动力学。

方法

在健康中国志愿者中进行了一项随机、双盲、安慰剂对照、单次递增剂量研究,志愿者接受了 101BHG-D01 鼻喷雾剂或安慰剂的鼻腔给药,剂量范围为 40µg 至 960µg(共 6 个剂量)。在预定时间点采集血样,并使用经过验证的高效液相色谱-串联质谱(HPLC-MS/MS)法测定血浆浓度。采用非房室法计算主要药代动力学参数,包括从零时到最后可测量浓度的时间的血浆浓度-时间曲线下面积(AUC)、从零时到无穷大的血浆浓度-时间曲线下面积(AUC)、最大血浆浓度(C)、最大血浆浓度时间(T)和消除半衰期(t)。通过监测不良事件、实验室检测、生命体征、体格检查、12 导联心电图(ECG)、前鼻镜检查、眼科检查和动态心电图监测来评估安全性。

结果

单次鼻内给药后,101BHG-D01 迅速吸收,中位 T 为 0.34-0.50 h,不同剂量组的平均 t 为 4.29-46.76 h,消除缓慢。在 40-960µg 检查剂量范围内,101BHG-D01 的 C 和 AUC 呈线性增加。101BHG-D01 鼻喷雾剂在健康中国受试者中耐受良好,所有不良事件均为轻度,研究期间未发生严重不良事件。

结论

在健康中国受试者中,以递增剂量单次鼻内给予 101BHG-D01 鼻喷雾剂安全且耐受良好。平均 C 和 AUC 与研究剂量成比例增加。101BHG-D01 鼻喷雾剂的药代动力学、安全性和耐受性特征表明,它是治疗鼻炎鼻漏的一个很好的候选药物。

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