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男性单次口服新型雄激素 11β-甲基-19-去甲睾酮-17β-十二烷酸酯的安全性和药代动力学。

Safety and Pharmacokinetics of Single-Dose Novel Oral Androgen 11β-Methyl-19-Nortestosterone-17β-Dodecylcarbonate in Men.

机构信息

Department of Medicine, University of Washington, Seattle, Washington.

Department of Medicine, Division of Endocrinology, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California.

出版信息

J Clin Endocrinol Metab. 2019 Mar 1;104(3):629-638. doi: 10.1210/jc.2018-01528.

Abstract

CONTEXT

11β-Methyl-19-nortestosterone-17β-dodecylcarbonate (11β-MNTDC) is an orally bioavailable prodrug of 11β-methyl-19-nortestosterone (11β-MNT) with androgenic and progestational activity.

OBJECTIVES

(i) Quantify 11β-MNT binding to androgen and progesterone receptors. (ii) Evaluate safety, tolerability, and serum gonadotropin and testosterone suppression by 11β-MNTDC in men.

DESIGN AND SETTING

(i) In vitro receptor binding and transactivation studies and (ii) randomized, double-blind, placebo-controlled single-dose, dose-escalating phase I study at two academic medical centers.

PARTICIPANTS AND INTERVENTION

Twelve healthy male volunteers were randomized (five active, one placebo) to escalating single oral doses (100, 200, 400, and 800 mg) of 11β-MNTDC or placebo given with or without food.

MAIN OUTCOME MEASURES

(i) In vitro 11β-MNT/11β-MNTDC human receptor binding and transactivation and (ii) safety and tolerability, pharmacokinetics, and quantification of serum gonadotropin and testosterone concentrations for 24 hours following dosing.

RESULTS

11β-MNT avidly binds and activates human androgen and progesterone receptors, but 11β-MNTDC has minimal activity. Single oral doses of 11β-MNTDC were well tolerated without serious adverse events. Administration of 11β-MNTDC with food markedly increased average 11β-MNTDC and 11β-MNT serum concentrations (P < 0.001 for all doses) compared with fasting with a significant dose-related effect on average serum drug concentrations (P < 0.0001). The 200-, 400-, and 800-mg doses significantly suppressed average serum testosterone concentrations (P < 0.05).

CONCLUSIONS

A single, oral dose of 11β-MNTDC up to 800 mg administered with food is safe and well tolerated in healthy men. The active drug 11β-MNT has androgenic and progestational activity, rapidly suppresses serum testosterone, and is a promising candidate for an effective once-daily oral male hormonal contraceptive.

摘要

背景

11β-甲基-19-去甲睾酮-17β-十二烷酸酯(11β-MNTDC)是具有雄激素和孕激素活性的 11β-甲基-19-去甲睾酮(11β-MNT)的口服生物利用前药。

目的

(i)定量测定 11β-MNT 与雄激素和孕激素受体的结合。(ii)评估 11β-MNTDC 在男性中的安全性、耐受性以及对血清促性腺激素和睾酮的抑制作用。

设计和设置

(i)体外受体结合和转激活研究,(ii)在两个学术医疗中心进行的随机、双盲、安慰剂对照、单次递增剂量、I 期研究。

参与者和干预

12 名健康男性志愿者随机分为(五名活性药物,一名安慰剂),接受递增的单次口服剂量(100、200、400 和 800mg)11β-MNTDC 或安慰剂,与或不与食物同时服用。

主要观察指标

(i)体外 11β-MNT/11β-MNTDC 人受体结合和转激活,(ii)安全性和耐受性、药代动力学以及给药后 24 小时内血清促性腺激素和睾酮浓度的定量。

结果

11β-MNT 强烈结合并激活了人雄激素和孕激素受体,但 11β-MNTDC 活性很小。11β-MNTDC 的单次口服剂量耐受性良好,无严重不良事件。与禁食相比,11β-MNTDC 与食物同时给药显著增加了平均 11β-MNTDC 和 11β-MNT 血清浓度(所有剂量均 P < 0.001),并且与平均血清药物浓度呈显著剂量相关性(P < 0.0001)。200、400 和 800mg 剂量显著抑制平均血清睾酮浓度(P < 0.05)。

结论

在健康男性中,单次口服 11β-MNTDC 高达 800mg 并与食物同时给药是安全且耐受良好的。活性药物 11β-MNT 具有雄激素和孕激素活性,可迅速抑制血清睾酮,是一种有前途的有效每日一次口服男性激素避孕药候选药物。

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