The Effect of Food on the Pharmacokinetics of Sildenafil after Single Administration of a Sublingual Testosterone and Oral Sildenafil Combination Tablet in Healthy Female Subjects.


Journal

The journal of sexual medicine
ISSN: 1743-6109
Titre abrégé: J Sex Med
Pays: Netherlands
ID NLM: 101230693

Informations de publication

Date de publication:
09 2019
Historique:
received: 18 12 2018
revised: 03 06 2019
accepted: 23 06 2019
entrez: 7 9 2019
pubmed: 7 9 2019
medline: 15 7 2020
Statut: ppublish

Résumé

Female sexual interest/arousal disorder (FSIAD) affects many women worldwide, but pharmacological treatment options are scarce. A new medicine being developed for FSIAD is an on-demand, dual-route, dual-release drug combination product containing 0.5 mg testosterone (T) and 50 mg sildenafil (S), referred to here as T+S. The aim of this study was to compare the effect of a fed and a fasted state on the pharmacokinetics of sildenafil following administration of T+S. Eighteen healthy women were administered T+S under fed and fasted conditions during 2 separate overnight visits in this randomized, open-label, balanced, 2-period, 2-treatment, 2-sequence crossover study. The pharmacokinetics of sildenafil and its active metabolite N-desmethyl sildenafil were determined over a 24-hour period. Total testosterone was assessed only at a limited number of time points for quality purposes, as sublingual uptake is not expected to be affected by food intake. The observed geometric mean ratios (GMRs) and 90% confidence intervals of sildenafil were not all contained within the prespecified bounds (0.80, 1.25). The GMR (90% CI) for plasma AUC The T+S combination tablet ruptures too late when taken in a fasted state and should therefore not be taken on an empty stomach. This is a well-controlled study that provides important insights into the performance characteristics of the delayed-release coating of the combination tablet. The higher variability of the pharmacokinetic parameters in the fasted state was caused by severely delayed rupture in one-third of the women. A reason for this is proposed but the present data do not explain this phenomenon. The pharmacokinetics of sildenafil from this modified-release tablet are more robust under fed conditions as compared to the artificial fasted condition where no food is consumed 10 hours prior to and 4 hours after dosing. The dosing situation under the tested fasting condition does not represent the expected common use of this product. Patients should, however, be instructed not to take the tablet on an empty stomach. Bloemers J, Gerritsen J, van Rooij K, et al. The Effect of Food on the Pharmacokinetics of Sildenafil After Single Administration of a Sublingual Testosterone and Oral Sildenafil Combination Tablet in Healthy Female Subjects. J Sex Med 2019; 19:1433-1443.

Identifiants

pubmed: 31488289
pii: S1743-6095(19)31274-3
doi: 10.1016/j.jsxm.2019.06.015
pii:
doi:

Substances chimiques

Vasodilator Agents 0
Testosterone 3XMK78S47O
Sildenafil Citrate BW9B0ZE037

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1433-1443

Informations de copyright

Copyright © 2019 International Society for Sexual Medicine. Published by Elsevier Inc. All rights reserved.

Auteurs

Jos Bloemers (J)

Emotional Brain BV, Almere, the Netherlands; Utrecht Institute for Pharmaceutical Sciences and Rudolf Magnus Institute of Neuroscience, Utrecht University, Utrecht, the Netherlands. Electronic address: j.bloemers@emotionalbrain.nl.

Jeroen Gerritsen (J)

Emotional Brain BV, Almere, the Netherlands.

Kim van Rooij (K)

Emotional Brain BV, Almere, the Netherlands; Utrecht Institute for Pharmaceutical Sciences and Rudolf Magnus Institute of Neuroscience, Utrecht University, Utrecht, the Netherlands.

Leo de Leede (L)

Exelion Bio-Pharmaceutical Consultancy BV, Waddinxveen, the Netherlands.

Ronald van der Geest (R)

3D-PharmXchange BV, Tilburg, the Netherlands.

Henderik W Frijlink (HW)

Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, Groningen, the Netherlands.

Hans P F Koppeschaar (HPF)

Emotional Brain BV, Almere, the Netherlands.

Berend Olivier (B)

Utrecht Institute for Pharmaceutical Sciences and Rudolf Magnus Institute of Neuroscience, Utrecht University, Utrecht, the Netherlands; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA; Groningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, the Netherlands.

Adriaan Tuiten (A)

Emotional Brain BV, Almere, the Netherlands.

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Classifications MeSH