Werkström Viktoria, Prothon Susanne, Ekholm Ella, Jorup Carin, Edsbäcker Staffan
AstraZeneca Global Medicines Development, Gothenburg, Sweden.
Department of Clinical and Experimental Pharmacology, Laboratory Medicines Unit, Lund University, Lund, Sweden.
Basic Clin Pharmacol Toxicol. 2016 Dec;119(6):574-581. doi: 10.1111/bcpt.12621. Epub 2016 Jul 8.
AZD5423 is a selective glucocorticosteroid receptor modulator developed for the inhaled use in asthma and COPD. This study reports the initial, first-in-man, single and repeat dose-escalating studies in healthy male individuals, including one cohort of male Japanese individuals. Inhaled, nebulized AZD5423 was safe and well tolerated up to and including the highest doses tested for up to 2 weeks of once-daily treatment. Plasma exposure suggested dose-proportional pharmacokinetics and dose-related effects on 24-hr plasma and urine cortisol. There were no or marginal effects on other biomarkers tested (osteocalcin, TRAP5b, DHEA-S and 4β-OH-cholesterol). No clinically relevant differences in safety or pharmacokinetics could be distinguished between the two study populations, although hypothalamus-pituitary-adrenal (HPA) effects appeared to be marginally greater in the Japanese- versus the Caucasian-dominant study population. AZD5423, inhaled via nebulization, can be used in healthy individuals at doses of at least 300 μg for 2 weeks. The effects on the HPA axis reported herein, together with efficacy data reported elsewhere, indicate that benefit-risk ratio may be improved relative to conventional inhaled steroids.
AZD5423是一种选择性糖皮质激素受体调节剂,开发用于哮喘和慢性阻塞性肺疾病(COPD)的吸入治疗。本研究报告了在健康男性个体中进行的首次人体、单次和重复剂量递增研究,其中包括一组日本男性个体。吸入雾化的AZD5423在每日一次治疗长达2周的情况下,直至并包括所测试的最高剂量,都是安全且耐受性良好的。血浆暴露表明其药代动力学呈剂量正比关系,且对24小时血浆和尿皮质醇有剂量相关效应。对其他测试生物标志物(骨钙素、抗酒石酸酸性磷酸酶5b、硫酸脱氢表雄酮和4β-羟基胆固醇)无影响或仅有轻微影响。尽管下丘脑-垂体-肾上腺(HPA)效应在以日本人群为主的研究组中似乎略高于以白种人群为主的研究组,但在两个研究人群之间未发现安全性或药代动力学方面的临床相关差异。通过雾化吸入的AZD5423可在健康个体中以至少300μg的剂量使用2周。本文报告的对HPA轴的影响,连同其他地方报告的疗效数据,表明与传统吸入性类固醇相比,其效益风险比可能得到改善。