Centre for Human Drug Research (CHDR), Zernikedreef 8, 2333 CL, Leiden, Netherlands; Leiden University Medical Centre (LUMC), Albinusdreef 2, 2333 ZA, Leiden, Netherlands.
Ferrer HealthTech, Diagonal 549, 08029, Barcelona, Spain.
Parkinsonism Relat Disord. 2022 Apr;97:84-90. doi: 10.1016/j.parkreldis.2022.02.014. Epub 2022 Mar 8.
Apomorphine is used to treat OFF periods in Parkinson's disease (PD) patients. AZ-009 is a novel apomorphine formulation that delivers a thermally-generated aerosol to the deep lung via inhalation with a single breath.
Part A was a randomized, placebo-controlled, double-blind study investigating the safety and pharmacokinetics of multiple ascending doses of AZ-009. PD patients (n = 24) received placebo or 2, 3 or 4 mg AZ-009 once daily for 5 days, followed by three times daily for 2 days with 2 h between doses. Part B was a double-blind crossover study in 8 PD patients who experience OFF periods. During an OFF state, patients received 4 mg AZ-009 and placebo on two consecutive days in a randomized order. MDS-UPDRS III and ON/OFF state were assessed pre- and post-dose.
Three times daily dosing with 2, 3 and 4 mg AZ-009 was relatively well tolerated with no apparent accumulation or changes in safety profile. Mild and transient throat irritation and cough were reported most often. AZ-009 was rapidly absorbed with median T between 1 and 2 min. When corrected for placebo response, the maximum effect of 4 mg AZ-009 based on MDS-UPDRS III scores was observed at 10 and 30 min post-dose with mean (SD) reductions of 6.8 (9.4) and 6.1 (9.1) points respectively. Whereas 0% of patients turned ON after placebo, 50% turned ON 10 min after 4 mg AZ-009 treatment.
AZ-009 is rapidly systemically absorbed and safe to dose three times daily. AZ-009 could provide a faster-acting and easier to use formulation than currently available therapies.
阿扑吗啡用于治疗帕金森病(PD)患者的关闭期。AZ-009 是一种新型阿扑吗啡制剂,通过单次呼吸将热产生的气雾剂输送到肺部深处。
A 部分是一项随机、安慰剂对照、双盲研究,旨在研究 AZ-009 多次递增剂量的安全性和药代动力学。24 名 PD 患者每天接受安慰剂或 2、3 或 4mg AZ-009 一次,连续 5 天,然后每天 3 次,两次给药之间间隔 2 小时。B 部分是 8 名经历关闭期的 PD 患者的双盲交叉研究。在关闭状态下,患者在连续两天内以随机顺序接受 4mg AZ-009 和安慰剂。给药前和给药后评估 MDS-UPDRS III 和 ON/OFF 状态。
每天 3 次服用 2、3 和 4mg AZ-009 耐受性良好,无明显蓄积或安全性状况变化。最常报告的是轻度和短暂的喉咙刺激和咳嗽。AZ-009 吸收迅速,中位 T 为 1 至 2 分钟。校正安慰剂反应后,基于 MDS-UPDRS III 评分,4mg AZ-009 的最大效应在给药后 10 和 30 分钟观察到,平均(SD)分别降低 6.8(9.4)和 6.1(9.1)点。虽然安慰剂后有 0%的患者转为 ON,但 4mg AZ-009 治疗后 10 分钟有 50%的患者转为 ON。
AZ-009 全身吸收迅速,每日 3 次给药安全。AZ-009 可能提供比现有疗法更快起效且更易于使用的制剂。