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磷酸二酯酶-9 抑制剂 E2027 的 1 期单上升和多上升剂量研究:路易体痴呆试验中目标结合的确认和 2 期剂量的选择。

Phase 1 Single Ascending and Multiple Ascending Dose Studies of Phosphodiesterase-9 Inhibitor E2027: Confirmation of Target Engagement and Selection of Phase 2 Dose in Dementia With Lewy Bodies Trial.

机构信息

Eisai Inc, Woodcliff Lake, NJ.

Eisai Co. Ltd., Tsukuba, Ibaraki, Japan.

出版信息

Alzheimer Dis Assoc Disord. 2022;36(3):200-207. doi: 10.1097/WAD.0000000000000515. Epub 2022 Jun 9.

DOI:10.1097/WAD.0000000000000515
PMID:35700341
Abstract

BACKGROUND

E2027 is a novel, highly selective and potent inhibitor of phosphodiesterase9 (PDE9) being evaluated as a treatment for dementia with Lewy bodies.

METHODS

Phase 1, randomized, double-blind, single ascending dose (SAD, n=96) and multiple ascending dose (MAD, n=68) studies evaluated E2027 doses (5 to 1200 mg) in healthy subjects. The impact of age, race (Japanese/non-Japanese), and food on pharmacokinetics (PK)/pharmacodynamics were evaluated. Serial cerebrospinal fluid (CSF) samples were collected to assess the target engagement.

RESULTS

E2027 PK profiles were biphasic (elimination half-life: ~30 hours. Approximately 3-fold accumulation was observed following multiple once-daily dosing. E2027 single doses of 50 to 400 mg resulted in mean maximum increases in CSF cyclic guanosine monophosphate ranging from 293% to 461% within 5.37 to 12.9 hours after dose administration to assess target engagement. Dose-response modelling of steady-state predose CSF cyclic guanosine monophosphate concentrations showed ≥200% increase from baseline is maintained with doses of ≥50 mg QD. The most common adverse events with E2027 were post-LP syndrome and back pain. PK profiles were similar between Japanese and non-Japanese. Higher exposure observed in fed versus fasted state was not considered clinically significant. PK exposure was higher in elderly subjects.

CONCLUSIONS

S.E2027 was well-tolerated following single and multiple administration. E2027 achieved maximal and sustained target engagement at 50 mg QD, the dose selected for the phase 2 clinical trial.

摘要

背景

E2027 是一种新型、高度选择性和强效的磷酸二酯酶 9(PDE9)抑制剂,正在作为治疗路易体痴呆的药物进行评估。

方法

在 1 期临床试验中,进行了随机、双盲、单次递增剂量(SAD,n=96)和多次递增剂量(MAD,n=68)研究,评估了健康受试者中 E2027 剂量(5 至 1200mg)。评估了年龄、种族(日本/非日本)和饮食对药代动力学(PK)/药效学的影响。采集连续的脑脊液(CSF)样本以评估目标结合情况。

结果

E2027 的 PK 特征呈双相(消除半衰期:约 30 小时。多次每日一次给药后观察到约 3 倍的蓄积。E2027 单次剂量为 50 至 400mg,在给药后 5.37 至 12.9 小时内,CSF 环鸟苷单磷酸的平均最大增加幅度为 293%至 461%,以评估目标结合情况。稳态预给药 CSF 环鸟苷单磷酸浓度的剂量反应模型表明,≥50mgQD 的剂量可维持≥200%的基线增加。E2027 最常见的不良反应是腰椎穿刺后综合征和背痛。PK 特征在日本人和非日本人之间相似。在进食状态下观察到的更高暴露量并不被认为具有临床意义。在老年受试者中观察到更高的 PK 暴露量。

结论

E2027 单次和多次给药后耐受性良好。E2027 在 50mgQD 时达到最大和持续的靶标结合,这是选择进行 2 期临床试验的剂量。

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