Formerly with Astellas Pharma Europe BV, Leiden, The Netherlands.
Astellas Pharma Global Development, Northbrook, Illinois, USA.
Clin Transl Sci. 2019 May;12(3):291-301. doi: 10.1111/cts.12618. Epub 2019 Feb 27.
Inhibition of the enzyme 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) represents a potential mechanism for improving pain conditions. ASP3662 is a potent and selective inhibitor of 11β-HSD1. Two phase I clinical studies were conducted to assess the safety, tolerability, pharmacokinetics (PKs), and pharmacodynamics (PDs) of single and multiple ascending doses of ASP3662 in healthy young and elderly non-Japanese and young Japanese subjects. Nonlinear, more than dose-proportional PKs were observed for ASP3662 after single-dose administration, particularly at lower doses (≤ 6 mg); the PKs at steady state were dose proportional, although the time to ASP3662 steady state was dose dependent at lower doses (≤ 2 mg). Similar PKs were observed among young Japanese, young non-Japanese, and elderly non-Japanese subjects. Specific inhibition of 11β-HSD1 occurred after both single and multiple doses of ASP3662. A marked dissociation between PKs and PDs was observed after single but not multiple doses of ASP3662. ASP3662 was generally safe and well tolerated.
抑制酶 11β-羟甾类脱氢酶 1(11β-HSD1)是改善疼痛状况的一种潜在机制。ASP3662 是一种有效的、选择性的 11β-HSD1 抑制剂。两项 I 期临床研究评估了 ASP3662 在健康的年轻和老年非日本以及年轻日本受试者中单次和多次递增剂量的安全性、耐受性、药代动力学(PKs)和药效动力学(PDs)。单次给药后,ASP3662 的 PKs 呈非线性、剂量依赖性,尤其是在较低剂量(≤6mg)时;稳态 PKs 呈剂量相关性,但在较低剂量(≤2mg)时,ASP3662 达到稳态的时间呈剂量依赖性。在年轻日本、年轻非日本和老年非日本受试者中观察到相似的 PKs。ASP3662 单次和多次给药后均可特异性抑制 11β-HSD1。ASP3662 单次给药后,PKs 和 PDs 之间出现明显的分离,但多次给药后则未出现。ASP3662 通常安全且耐受良好。