Astellas Pharma Inc., Tokyo, Japan.
Astellas Pharma Europe B.V., Leiden, The Netherlands.
Clin Pharmacol Drug Dev. 2024 Oct;13(10):1130-1142. doi: 10.1002/cpdd.1460. Epub 2024 Aug 9.
ASP8302 is an orally administered positive allosteric modulator of the muscarinic M receptor. Two Phase 1 studies were conducted, a first-in-human study in Europe and a Japanese phase 1 study. Both were randomized, participant- and investigator-blinded, placebo-controlled, single and multiple ascending oral doses, parallel group, clinical studies in healthy volunteers. Both studies evaluated safety and pharmacokinetics and also included salivary secretion and pupil diameter as pharmacodynamic assessments. There were no deaths, serious adverse events, or treatment-emergent adverse events reported leading to study discontinuation. There were no clinically relevant findings in any of the laboratory, vital signs, electrocardiogram assessments, or photosensitivity testing following multiple administration of up to 150 mg or up to 140 mg once daily for 14 days in the European first-in-human and Japanese Phase 1 study, respectively. The pharmacokinetics of ASP8302 were approximately linear over the dose range studied. There was no evidence of drug accumulation upon repeated dosing. In both studies, ASP8302 showed a dose-dependent pharmacodynamic effect on saliva production at doses from 100 mg onward, which was maintained during repeated dosing. No effect was observed on pupil diameter. These data supported progression of ASP8302 into Phase 2 clinical trials for further clinical development.
ASP8302 是一种口服的毒蕈碱 M 受体的正变构调节剂。进行了两项 1 期研究,一项是在欧洲进行的首次人体研究,另一项是日本的 1 期研究。这两项研究均为随机、双盲(参与者和研究者)、安慰剂对照、单次和多次递增口服剂量、平行组的健康志愿者临床研究。这两项研究均评估了安全性和药代动力学,还包括唾液分泌和瞳孔直径作为药效学评估。没有报告导致研究中止的死亡、严重不良事件或治疗后出现的不良事件。在欧洲首次人体研究和日本 1 期研究中,分别多次给予高达 150mg 或高达 140mg 每日一次连续 14 天,在任何实验室、生命体征、心电图评估或光致敏性试验中均无临床相关发现。ASP8302 的药代动力学在研究的剂量范围内呈近似线性。重复给药时无药物蓄积的证据。在这两项研究中,ASP8302 在 100mg 及以上剂量时显示出剂量依赖性的唾液产生药效学效应,在重复给药期间得到维持。对瞳孔直径没有观察到影响。这些数据支持 ASP8302 进入 2 期临床试验,以进一步进行临床开发。