Literature DB >> 20097934

Pharmacokinetics of dapoxetine hydrochloride in healthy Chinese, Japanese, and Caucasian men.

An Thyssen1, Om Sharma, Si Tianmei, Joseph W Aquilina, An Vandebosch, Shean-Sheng Wang, Ramagopal Mudumbi, Hsiu-Ling Hsiao.   

Abstract

Dapoxetine is a short-acting selective serotonin reuptake inhibitor developed for the on-demand treatment of premature ejaculation and is approved in some European Union countries, as well as Mexico and Korea, for this indication. The pharmacokinetics of dapoxetine 30 mg and 60 mg in healthy Chinese (single dose), Japanese, and Caucasian men (single and multiple dose) were assessed in 2 studies. In the 3 ethnic groups, dapoxetine was rapidly absorbed following oral administration, with peak plasma concentrations evident approximately 1 hour after dosing, independent of dose, dosing frequency (single or multiple dosing), or ethnicity. Dapoxetine was eliminated in a biphasic manner with an apparent mean terminal half-life of 14 to 17 hours. There was a dose-proportional increase in dapoxetine maximum plasma concentration (C(max)) and area under concentration-time curves (AUCs). The single-dose pharmacokinetic parameters of dapoxetine metabolites were also similar for the 3 ethnic groups, as were the pharmacokinetics of dapoxetine and its metabolites following single and multiple dosing in Caucasian and Japanese men. Dapoxetine was well tolerated by all 3 ethnic groups.

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Year:  2010        PMID: 20097934     DOI: 10.1177/0091270009359183

Source DB:  PubMed          Journal:  J Clin Pharmacol        ISSN: 0091-2700            Impact factor:   3.126


  7 in total

1.  Dapoxetine: a new option in the medical management of premature ejaculation.

Authors:  Chris G McMahon
Journal:  Ther Adv Urol       Date:  2012-10

Review 2.  Dapoxetine: in premature ejaculation.

Authors:  Sheridan M Hoy; Lesley J Scott
Journal:  Drugs       Date:  2010-07-30       Impact factor: 9.546

3.  Zein-alpha lipoic acid-loaded nanoparticles to enhance the oral bioavailability of dapoxetine: optimization and clinical pharmacokinetic evaluation.

Authors:  Khalid M El-Say; Osama Aa Ahmed; Amir I Mohamed; Martin K Safo; Abdelsattar M Omar
Journal:  Int J Nanomedicine       Date:  2019-09-12

4.  Cardiovascular safety profile of dapoxetine during the premarketing evaluation.

Authors:  Peter R Kowey; Ramagopal V Mudumbi; Joseph W Aquilina; Peter M DiBattiste
Journal:  Drugs R D       Date:  2011

5.  Dapoxetine: an evidence-based review of its effectiveness in treatment of premature ejaculation.

Authors:  Ej McCarty; Ww Dinsmore
Journal:  Core Evid       Date:  2012-01-19

6.  Efficacy of dapoxetine in the treatment of premature ejaculation.

Authors:  Chris G McMahon
Journal:  Clin Med Insights Reprod Health       Date:  2011-08-02

7.  Comparison of paroxetine and dapoxetine, a novel selective serotonin reuptake inhibitor in the treatment of premature ejaculation.

Authors:  Abdulmuttalip Simsek; Sinan Levent Kirecci; Onur Kucuktopcu; Faruk Ozgor; Mehmet Fatih Akbulut; Omer Sarilar; Unsal Ozkuvanci; Zafer Gokhan Gurbuz
Journal:  Asian J Androl       Date:  2014 Sep-Oct       Impact factor: 3.285

  7 in total

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