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17α-炔基 3α, 17β-雄烷二醇的非临床和临床药理学、药代动力学和代谢。

17α-alkynyl 3α, 17β-androstanediol non-clinical and clinical pharmacology, pharmacokinetics and metabolism.

机构信息

Harbor BioSciences, Inc., 9171 Towne Centre Drive, Suite 181, San Diego, CA 92122, USA.

出版信息

Invest New Drugs. 2012 Feb;30(1):59-78. doi: 10.1007/s10637-010-9517-0. Epub 2010 Sep 3.

Abstract

17α-ethynyl-5α-androstane-3α, 17β-diol (HE3235, Apoptone) is an orally bioavailable synthetic analogue of 3β-androstanediol, that is active in rodent models of prostate and breast cancer, and is in Phase IIa clinical trials for the treatment of early- and late-stage prostate cancer. In preparation for clinical studies, nuclear hormone receptor and P450 interactions for HE3235 and major metabolites were characterized in vitro, and pharmacokinetics and metabolite profiles were studied in rodents, dogs, and monkeys. Four-week safety studies conducted in rats and dogs indicated a substantial margin of safety for clinical use, and no evidence of electrocardiographic or neurological effects, although anorexia, thrombocytopenia, and hypokalemia were identified as potentially dose-limiting toxicities at superpharmacological exposures. Pharmacokinetics and drug metabolism have been studied in prostate cancer patients.

摘要

17α-乙炔基-5α-雄烷-3α,17β-二醇(HE3235,凋亡酮)是一种可口服生物利用的 3β-雄烷二醇合成类似物,在前列腺癌和乳腺癌的啮齿动物模型中具有活性,目前正在进行治疗早期和晚期前列腺癌的 IIa 期临床试验。为准备临床研究,在体外对 HE3235 及其主要代谢物与核激素受体和 P450 的相互作用进行了表征,并在啮齿动物、狗和猴子中研究了药代动力学和代谢物特征。在大鼠和狗中进行的为期 4 周的安全性研究表明,临床使用具有很大的安全性,没有心电图或神经影响的证据,尽管在超药理学暴露下,厌食、血小板减少症和低钾血症被确定为潜在的剂量限制毒性。已在前列腺癌患者中研究了药代动力学和药物代谢。

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