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首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Multiple-dose, safety, pharmacokinetics, and pharmacodynamics of a new selective estrogen receptor modulator, ERA-923, in healthy postmenopausal women.
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Multiple-dose, safety, pharmacokinetics, and pharmacodynamics of a new selective estrogen receptor modulator, ERA-923, in healthy postmenopausal women.

机译:新的选择性雌激素受体调节剂ERA-923在绝经后健康女性中的多剂量,安全性,药代动力学和药效学。

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摘要

ERA-923 is a new selective estrogen receptor modulator under clinical investigation for use in tamoxifen refractory metastatic breast cancer. This study evaluated the safety, tolerability, pharmacokinetics, and pharmacodynamics of once-daily oral ERA-923 (10-200 mg) for 28 days in healthy postmenopausal females. ERA-923 was well tolerated, and adverse events were mild and reversible. No clinically significant changes in laboratory values were found with ERA-923 versus placebo. ERA-923 appeared to undergo extensive metabolism and enterohepatic recirculation. In addition, pharmacokinetic analysis showed that a high-fat breakfast increased the extent of absorption. ERA-923-dosed subjects had no uterine or ovarian changes when evaluated with transvaginal ultrasound and compared to placebo subjects. Overall, ERA-923 was safe and well tolerated in postmenopausal women dosed for 28 days.
机译:ERA-923是一种新的选择性雌激素受体调节剂,正在临床研究中,用于他莫昔芬难治性转移性乳腺癌。这项研究评估了健康绝经后女性每天口服ERA-923(10-200 mg)28天的安全性,耐受性,药代动力学和药效学。 ERA-923的耐受性良好,不良事件轻微且可逆。与安慰剂相比,ERA-923没有发现实验室值的临床显着变化。 ERA-923似乎经历了广泛的新陈代谢和肝肠循环。另外,药代动力学分析表明高脂早餐增加了吸收程度。经阴道超声评估并与安慰剂相比,ERA-923给药的受试者无子宫或卵巢变化。总体而言,ERA-923对停经28天的绝经后妇女安全且耐受良好。

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