Literature DB >> 33528113

Pharmacokinetics and Safety of Dapoxetine Hydrochloride in Healthy Chinese Men: Impact of Dose and High-Fat Meal.

Jingyan Liu1, Zhihui Li1, Keyu Yan1, Gehang Ju1, Wen Qiu1.   

Abstract

Dapoxetine is the first oral medication specifically developed for the on-demand treatment of premature ejaculation. The pharmacokinetics and safety of 30 mg (n = 40) and 60 mg (n = 38) dapoxetine in healthy Chinese under fasted and fed states were assessed in 2 studies. Both studies are random, single-center, 2-period, open-label, 2-way crossover designs. Plasma concentration of dapoxetine was determined by high-performance liquid chromatography-tandem mass spectrometry, and the pharmacokinetic parameters were calculated using noncompartmental analysis. Dapoxetine was quickly absorbed and reached maximum concentration 1 to 3 hours after oral administration. Elimination was biphasic, and the plasma concentration decreased to 3% to 7% of maximum concentration by 24 hours while half-life was 15 to 18 hours. Meantime, high-fat meals slightly increased its exposure. Both doses of dapoxetine were well tolerated. The adverse events in the high-dose group under fasted and fed states were 37.9% and 19.0%, respectively.
© 2021, The American College of Clinical Pharmacology.

Entities:  

Keywords:  dapoxetine; dose proportion; food effect; pharmacokinetics; premature ejaculation; safety

Mesh:

Substances:

Year:  2021        PMID: 33528113     DOI: 10.1002/cpdd.919

Source DB:  PubMed          Journal:  Clin Pharmacol Drug Dev        ISSN: 2160-763X


  1 in total

1.  Determination of Dapoxetine Hydrochloride in Human Plasma by HPLC-MS/MS and Its Application in a Bioequivalence Study.

Authors:  Xin Zhang; Zhanwang Gao; Fei Qin; Kehan Chen; Jiansong Wang; Lingli Wang
Journal:  Molecules       Date:  2022-04-22       Impact factor: 4.411

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.