Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of a Muscarinic M3 Receptor-Positive Allosteric Modulator ASP8302 Following Single and Multiple Ascending Oral Doses in Healthy Volunteers.

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Clinical Pharmacology in Drug Development Pub Date : 2024-10-01 Epub Date: 2024-08-09 DOI:10.1002/cpdd.1460
Shin Takusagawa, Nicoline Treijtel, Masako Saito, Ingrid Michon, Daisuke Miyatake, Fumio Osaki, Sayuri Guro, Tomasso Fadini, Hisakuni Sekino, Marlous Aarden-Bakker, Kentaro Kuroishi, Jan Willem Olivier van Till, Dorien Groenendaal-van de Meent, Michiel de Vries
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Abstract

ASP8302 is an orally administered positive allosteric modulator of the muscarinic M3 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.

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在健康志愿者中单次和多次递增口服剂量后,肌卡因 M3 受体阳性异构调节剂 ASP8302 的安全性、耐受性、药代动力学和药效学。
ASP8302 是一种口服的毒蕈碱 M3 受体正异位调节剂。目前已进行了两项 1 期研究,一项是欧洲的首次人体研究,另一项是日本的 1 期研究。这两项研究都是在健康志愿者中进行的随机、参与者和研究者双盲、安慰剂对照、单次和多次递增口服剂量、平行组临床研究。两项研究都对安全性和药代动力学进行了评估,还包括唾液分泌和瞳孔直径等药效学评估。没有导致研究中止的死亡、严重不良事件或治疗突发不良事件的报告。在欧洲的首次人体试验和日本的1期研究中,分别多次给药最高150毫克或最高140毫克,每天1次,连续14天后,实验室、生命体征、心电图评估或光敏试验均未出现任何临床相关结果。在研究的剂量范围内,ASP8302的药代动力学近似线性。在重复给药时,没有证据表明存在药物蓄积。在这两项研究中,从 100 毫克剂量开始,ASP8302 对唾液分泌具有剂量依赖性药效学效应,这种效应在重复给药过程中保持不变。没有观察到对瞳孔直径的影响。这些数据支持 ASP8302 进入第二阶段临床试验,以进一步进行临床开发。
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来源期刊
CiteScore
3.70
自引率
10.00%
发文量
154
期刊介绍: Clinical Pharmacology in Drug Development is an international, peer-reviewed, online publication focused on publishing high-quality clinical pharmacology studies in drug development which are primarily (but not exclusively) performed in early development phases in healthy subjects.
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