制剂对度他雄胺药代动力学特征的影响。 - Suppr

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超能文献

Impact of Formulation on the Pharmacokinetic Profile of Dutasteride.

作者信息

Michel Martin C

机构信息

Department of Pharmacology, Johannes Gutenberg University, Obere Zahlbacher Str. 67, 55131, Mainz, Germany.

出版信息

Clin Drug Investig. 2016 Sep;36(9):769-770. doi: 10.1007/s40261-016-0429-4.

DOI:10.1007/s40261-016-0429-4

PMID:27364517

Abstract

摘要

相似文献

Impact of Formulation on the Pharmacokinetic Profile of Dutasteride.制剂对度他雄胺药代动力学特征的影响。

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Formulation and in vivo evaluation of a self-microemulsifying drug delivery system of dutasteride.度他雄胺自微乳化药物递送系统的制剂与体内评价

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Design of a gelatin microparticle-containing self-microemulsifying formulation for enhanced oral bioavailability of dutasteride.含明胶微粒的自微乳化制剂设计用于提高度他雄胺的口服生物利用度

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Biomed Mater Eng. 2014;24(1):571-9. doi: 10.3233/BME-130844.

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Arch Ital Urol Androl. 2013 Dec 31;85(4):200-6. doi: 10.4081/aiua.2013.4.200.

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本文引用的文献

Impact of Formulation on the Pharmacokinetics of Dutasteride: Results from Two Phase I Studies.制剂对度他雄胺药代动力学的影响：两项I期研究的结果

Clin Drug Investig. 2016 Sep;36(9):763-767. doi: 10.1007/s40261-016-0419-6.

Efficacy and safety of a fixed-dose combination of dutasteride and tamsulosin treatment (Duodart(®) ) compared with watchful waiting with initiation of tamsulosin therapy if symptoms do not improve, both provided with lifestyle advice, in the management of treatment-naïve men with moderately symptomatic benign prostatic hyperplasia: 2-year CONDUCT study results.度他雄胺与坦索罗辛固定剂量复方制剂（Duodart®）治疗初治的中度症状性良性前列腺增生男性患者的疗效和安全性，与症状未改善时开始坦索罗辛治疗并给予生活方式建议的观察等待策略相比：2年CONDUCT研究结果

BJU Int. 2015 Sep;116(3):450-9. doi: 10.1111/bju.13033. Epub 2015 Jan 29.

Pharmacokinetic bioequivalence studies of a fixed-dose combination of tamsulosin and dutasteride in healthy volunteers.坦索罗辛与度他雄胺固定剂量复方制剂在健康志愿者中的药代动力学生物等效性研究。

Clin Drug Investig. 2014 May;34(5):335-49. doi: 10.1007/s40261-014-0179-0.

EAU guidelines on the treatment and follow-up of non-neurogenic male lower urinary tract symptoms including benign prostatic obstruction.EAU 指南：非神经原性男性下尿路症状（包括良性前列腺梗阻）的治疗和随访。

Eur Urol. 2013 Jul;64(1):118-40. doi: 10.1016/j.eururo.2013.03.004. Epub 2013 Mar 13.

The effects of combination therapy with dutasteride and tamsulosin on clinical outcomes in men with symptomatic benign prostatic hyperplasia: 4-year results from the CombAT study.度他雄胺和坦索罗辛联合治疗对有症状的良性前列腺增生症男性临床结局的影响：来自 CombAT 研究的 4 年结果。

Eur Urol. 2010 Jan;57(1):123-31. doi: 10.1016/j.eururo.2009.09.035. Epub 2009 Sep 19.

Glibenclamide transdermal patches: physicochemical, pharmacodynamic, and pharmacokinetic evaluations.格列本脲透皮贴剂：物理化学、药效学及药代动力学评价

J Pharm Sci. 2004 Jun;93(6):1577-94. doi: 10.1002/jps.20058.

The long-term effect of doxazosin, finasteride, and combination therapy on the clinical progression of benign prostatic hyperplasia.多沙唑嗪、非那雄胺及联合治疗对良性前列腺增生临床进展的长期影响。

N Engl J Med. 2003 Dec 18;349(25):2387-98. doi: 10.1056/NEJMoa030656.

Dutasteride.度他雄胺

Drugs Aging. 2003;20(12):905-16; discussion 917-8. doi: 10.2165/00002512-200320120-00005.

Efficacy and tolerability of doxazosin and finasteride, alone or in combination, in treatment of symptomatic benign prostatic hyperplasia: the Prospective European Doxazosin and Combination Therapy (PREDICT) trial.多沙唑嗪与非那雄胺单独或联合使用治疗有症状的良性前列腺增生的疗效和耐受性：欧洲多沙唑嗪前瞻性联合治疗（PREDICT）试验

Urology. 2003 Jan;61(1):119-26. doi: 10.1016/s0090-4295(02)02114-3.

Sustained-release alfuzosin, finasteride and the combination of both in the treatment of benign prostatic hyperplasia. European ALFIN Study Group.

Eur Urol. 1998 Sep;34(3):169-75. doi: 10.1159/000019706.

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