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