Dapoxetine

Dapoxetine, marketed as Priligy, is a medication used for the treatment of premature ejaculation (PE) in men 18–64 years old.[2][3] Dapoxetine works by inhibiting the serotonin transporter, increasing serotonin's action at the post synaptic cleft, and as a consequence promoting ejaculatory delay.[4] As a member of the selective serotonin reuptake inhibitor (SSRI) family, dapoxetine was initially created as an antidepressant. However, unlike other SSRIs, dapoxetine is absorbed and eliminated rapidly in the body. Its fast acting property makes it suitable for the treatment of PE but not as an antidepressant.[5]

Dapoxetine
Clinical data
Trade namesPriligy, others (see below)
AHFS/Drugs.comInternational Drug Names
Routes of
administration		Oral (tablets)
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability15–76% (mean 42%), Tmax = 1–1.3 hours
Protein binding>99%
MetabolismLiver (CYP2D6, CYP3A4), kidney (FMO1)
MetabolitesDapoxetine-N-oxide, desmethyldapoxetine, didesmethyldapoxetine
Elimination half-life1.5–1.6 h
ExcretionKidneys[1]
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC21H23NO
Molar mass305.421 g·mol−1
3D model (JSmol)

Originally created by Eli Lilly pharmaceutical company, dapoxetine was sold to Johnson & Johnson in 2003 and submitted as a New Drug Application to the Food and Drug Administration (FDA) for the treatment of PE in 2004.[6] Dapoxetine is sold in several European and Asian countries, and in Mexico. In the US, dapoxetine has been in phase III development. In May 2012, USA-based Furiex Pharmaceuticals reached an agreement with ALZA Corp and Janssen Pharmaceutica to market dapoxetine in the USA, Japan and Canada, while selling the rights to market the drug in Europe, most of Asia, Africa, Latin America and the Middle East to Menarini.[7]

Medical uses

Premature ejaculation

Randomized, double blind, placebo-controlled trials have confirmed the efficacy of dapoxetine for the treatment of PE.[8] Different dosage has different impacts on different types of PE. Dapoxetine 60 mg significantly improves the mean intravaginal ejaculation latency time (IELT) compared to that of dapoxetine 30 mg in men with lifelong PE, but there is no difference in men with acquired PE.[9] Dapoxetine, given 1–3 hours before sexual episode, prolongs IELT and increases the sense of control and sexual satisfaction in men of 18 to 64 years of age with PE. Since PE is associated with personal distress and interrelationship difficulty, dapoxetine provides help for men with PE to overcome this condition.[10] With no drug approved specifically for treatment for PE in the US and some other countries, other SSRIs such as fluoxetine, paroxetine, sertraline, fluvoxamine, and citalopram have been used off-label to treat PE. Waldinger's meta-analysis shows that the use of these conventional antidepressants increases IELT two- to nine-fold above baseline, compared to three- to eight-fold when dapoxetine is used.[9] However, these SSRIs may need to be taken daily in order to achieve meaningful efficacy, and their comparatively longer half-lives increase the risk of drug accumulation and a corresponding increase of adverse effects such as reduced libido.[11] Dapoxetine, on the other hand, is generally categorized as a fast-acting SSRI. It is more rapidly absorbed and mostly eliminated from the body within a few hours. These pharmacokinetics are more favorable in that they might minimize drug accumulation in the body, habituation, and side effects.[5]

Contraindications

Dapoxetine should not be used in men with moderate to severe hepatic impairment and in those receiving CYP3A4 inhibitors such as ketoconazole, ritonavir, and telithromycin. Dapoxetine can also not be used in patients with heart failure, permanent pacemaker, or other significant ischemic heart disease. Caution is advised in men receiving thioridazine, monoamine oxidase inhibitors, SSRIs, serotonin-norepinephrine reuptake inhibitors, or tricyclic antidepressant. If a patient stops taking one of these drugs, he should wait for 14 days before taking dapoxetine. If a patient stops taking dapoxetine, he should wait for 7 days before receiving these drugs.[4]

Adverse effects

The most common effects when taking dapoxetine are nausea, dizziness, dry mouth, headache, diarrhea, and insomnia.[12][13] Discontinuation due to adverse effects is dose related. According to McMahon in recent study in Asia, the rate of discontinuation is 0.3%, 1.7%, and 5.3% of 1067 studied subjects with placebo, dapoxetine 30 mg, and dapoxetine 60 mg respectively.[14] Unlike other SSRIs used to treat depression, which have been associated with high incidences of sexual dysfunction,[15] dapoxetine is associated with low rates of sexual dysfunction. Taken as needed, dapoxetine has very mild adverse effects of decreased libido (<1%) and erectile dysfunction (<4%).[5]

Overdose

No case of drug overdose has been reported during clinical trials.[16]

Interactions

With phosphodiesterase inhibitors (PDE5 inhibitors)

Many men that have PE also suffer from erectile dysfunction (ED). Treatment for these patients should consider the drug–drug interaction between dapoxetine and PDE5 inhibitors such as tadalafil (Cialis) or sildenafil (Viagra). In Dresser study (2006), plasma concentration of 24 subjects was obtained. Half of the sample pool were treated with dapoxetine 60 mg + tadalafil 20 mg; the other half were treated with dapoxetine 60 mg + sildenafil 100 mg. These plasma samples were then analyzed using liquid chromatography-tandem mass spectrometry. The results showed that dapoxetine does not alter the pharmacokinetic of tadalafil or sildenafil.[2]

With ethanol

Ethanol doesn't affect the pharmacokinetics of dapoxetine when taking concurrently.[17]

Mechanism of actions

The mechanism through which dapoxetine affects premature ejaculation is still unclear. However, it is presumed that dapoxetine works by inhibiting serotonin transporter and subsequently increasing serotonin's action at pre and postsynaptic receptors[18] Human ejaculation is regulated by various areas in the central nervous system (CNS).[19] The ejaculatory pathway originates from spinal reflex at the thoracolumbar and lumbosacral level of spinal cord activated by stimuli from male genital. These signals are relayed to the brain stem, which then is influenced by a number of nuclei in the brain such as medial preoptic and paraventricular nulcei.[20] Clement's study performed on anaesthetized male rats showed that acute administration of dapoxetine inhibits ejaculatory expulsion reflex at supraspinal level by modulating activity of lateral paragigantocellular nucleus (LPGi) neurons. These effects cause an increase in pudendal motoneuron reflex discharge (PMRD) latency. However, it is unclear whether dapoxetine acts directly on LPGi or on the descending pathway in which LPGi located.[21]

Pharmacokinetics
Absorption

Dapoxetine is a white powder substance and water- insoluble. Taken 1–3 hours before sexual activity, it is rapidly absorbed in the body. Its maximum plasma concentration (Cmax) is reached 1–2 hours after oral administration. The Cmax and AUC (Area Under the plasma vs. time Curve) are dose dependent. The Cmax and Tm (time needed to obtain the maximum plasma concentration) after single doses of dapoxetine 30 mg and 60 mg are 297 and 498 ng/mL at 1.01 and 1.27 hours respectively. A high fat meal does reduce the Cmax slightly, but it is insignificant. In fact, food doesn't alter dapoxetine pharmacokinetics. Dapoxetine can be taken with or without food.[22]

Distribution

Dapoxetine is absorbed and distributed rapidly in the body. Greater than 99% of dapoxetine is bound to the plasma protein. The mean steady state volume is 162 L. Its initial half-life is 1.31 hours (30 mg dose) and 1.42 hours (60 mg dose,) and its terminal half life is 18.7 hours (30 mg dose) and 21.9 hours (60 mg dose).[23]

Metabolism

Dapoxetine is metabolized extensively in the liver and kidney by multiple enzymes such as CYP2D6, CYP3A4, and flavin monooxygenase 1 (FMO1). The major product at the end of the metabolic pathway is circulating dapoxetine N-oxide, which is a weak SSRI and contributes no clinical effect. The other products presented less than 3% in the plasma are desmethyldapoxetine and didesmethydapoxetine. Desmethyldapoxetine is approximately equipotent to dapoxetine.[24]

Excretion

The metabolites of dapoxetine are eliminated rapidly in the urine with a terminal half-life of 18.7 and 21.9 hours for a single dose of 30 mg and 60 mg respectively.[17]

Safety and tolerability
Cardiovascular safety

The cardiovascular safety profile of dapoxetine has been studied extensively during the drug development. Phase I trials showed that dapoxetine had neither clinical significant electrocardiographic effects nor delayed repolarization effects, with dosing up to four-fold greater than the maximum recommended dosage which is 60 mg. Phase III studies in men with PE showed a safety and well tolerate profile of dapoxetine with dosing of 30 and 60 mg. There is no cardiovascular adverse had been found.[25]

Neurocognitive safety

Studies of SSRIs in patients with major psychiatric disorders prove that SSRIs are potentially associated with certain neurocognitive adverse effects such as anxiety, akathisia, hypomania, changes in mood, or suicidal thought.[26][27] However, there is no study on the effects of SSRIs in men with PE. McMahon's study in 2012 showed that dapoxetine has no effect on mood and is not associated with anxiety or suicidality.[28]

Withdrawal syndrome

The incidence of antidepressant discontinuation syndrome symptoms in men using dapoxetine to treat premature ejaculation has been described by reviewers as low or no different from the incidence of such symptoms in men withdrawn from placebo treatment.[29][29][30] The lack of chronic serotonergic stimulation with on-demand dapoxetine minimizes the potentiation action of serotonin at synaptic cleft, thus decreasing the risk of DESS.[31]

Synthesis
Synthesis of dapoxetine

Currently very few methods are used to synthesize (S)-dapoxetine. This novel approach consists of only six steps in which three main steps are shown above. The initial reactant is trans-cinnamyl alcohol which is commercial available. Sharpless asymmetric epoxidation and Mitsunobu reaction have been used to produce expected (S)-dapoxetine. The overall yield is 35%. This method is considered a good choice compare to the known methods due to high yield and easily obtainable reactants.[32]

Regulatory history

Dapoxetine was created by Eli Lilly and in phase I clinical trial as an antidepressant. However, it never worked out well as a medication for the treatment of depression and was shelved for a while before subsequently developed to treat PE. In December 2003, Eli Lilly sold patent of dapoxetine to Pharmaceutical Product Development (PPD) for 65 million US dollars in cash. Eli Lilly may also receive royalties payment from PPD if the sale exceeds certain amount.

ALZA is the current owner of dapoxetine. However, PPD will receive milestone payment and drug royalties from ALZA. If approved, dapoxetine will be marketed in the US by Ortho McNeil pharmaceutical, Inc. Ortho McNeil as well as Janssen-Ortho Inc, or Janssen-Cilag are all units of Johnson & Johnson. As at 2005, Dapoxetine was in phase III clinical trials, pending review by the Federal Drug Administration (FDA).[33]

Dapoxetine has been marketed and approved in more than 50 countries.[34] Dapoxetine has been approved in Italy, Spain, Mexico, South Korea, and New Zealand in 2009 and 2010; marketed in Sweden, Austria, Germany, Finland, Spain, Portugal, and Italy. It has also been approved in France, Russia, Malaysia, Philippines, Argentina, and Uruguay.[4]

Trade names

Dapoxetine is sold under a variety of brand names including Dumax, Duratia, Joypox (from daPOXetine), Kutub, Lejam, Longride Pentenal-30, Priligy, Sustinex, Ever Long, Joytab, Dapo, Westoxetin,Primaxetin (Примаксетин) in Russia and Exirect (in Iran).

gollark: I had vaguely assumed it was basically radar or something, and the X-raying let them know density (ish).
gollark: Arguably it was me. However, this is you, as a result.
gollark: Indeed. It's really convenient.
gollark: Yes, everyone else should share my preferences or they're wrong.
gollark: I don't think you know how preferences work.

See also

References
  1. "Russian State Register of Medicines. Priligy (dapoxetine) Film-coated Tablets, for Oral Use. Full Prescribing Information" (in Russian). 25 July 2013. Retrieved 11 August 2016. Cite journal requires |journal= (help)
  2. Dresser, M. J.; Desai, D.; Gidwani, S.; Seftel, A. D. & Modi, N. B. (2006). "Dapoxetine, a novel treatment for premature ejaculation, does not have pharmacokinetic interactions with phosphodiesterase-5 inhibitors". International Journal of Impotence Research. 18 (1): 104–110. doi:10.1038/Sj.Ijir.3901420. PMID 16307008.
  3. McMahon, CG (Oct 2012). "Dapoxetine: a new option in the medical management of premature ejaculation". Therapeutic Advances in Urology. 4 (5): 233–51. doi:10.1177/1756287212453866. PMC 3441133. PMID 23024705.
  4. Government, A. ( 2010). Australian Public Assessment Report for Dapoxetine (D. o. H. a. A. T. G. Administration, Trans.).
  5. Andersson, K. E.; Mulhall, J. P. & Wyllie, M. G. (2006). "Pharmacokinetic and pharmacodynamic features of dapoxetine, a novel drug for 'on-demand' treatment of premature ejaculation". BJU International. 97 (2): 311–315. doi:10.1111/J.1464-410x.2006.05911.X. PMID 16430636.
  6. McCarty, E. & Dinsmore, W. (2012). "Dapoxetine: an evidence-based review of its effectiveness in treatment of premature ejaculation". Core Evid. 7: 1–14. doi:10.2147/CE.S13841. PMC 3273363. PMID 22315582.
  7. "Furiex Pharma gets rights to Priligy, some of which it sells on to Menarini". The Pharma Letter. 15 May 2012. Retrieved 11 February 2020.
  8. McMahon, C. G.; McMahon, C. N.; Leow, L. J. (2006). "New agents in the treatment of premature ejaculation". Neuropsychiatr Dis Treat. 2 (4): 489–503. doi:10.2147/nedt.2006.2.4.489. PMC 2671940. PMID 19412497.
  9. Pryor, J. L.; Althof, S. E.; Steidle, C.; Rosen, R. C.; Hellstrom, W. J. G.; Shabsigh, R.; Kell, S. (2006). "Efficacy and tolerability of dapoxetine in treatment of premature ejaculation: an integrated analysis of two double-blind, randomized controlled trials". Lancet. 368 (9539): 929–937. doi:10.1016/s0140-6736(06)69373-2. PMID 16962882.
  10. Shabsigh, R.; Broderick, G. A.; Miloslavsky, M.; Bull, S. (2006). "Dapoxetine has long-term efficacy in the treatment of premature ejaculation". Journal of Urology. 175 (4): 297–298.
  11. Montague, D. K.; Jarow, J.; Broderick, G. A.; Dmochowski, R. R.; Heaton, J. P.; Lue, T. F.; Sharlip, I. D. (2004). "AUA guideline on the pharmacologic management of premature ejaculation. [Guideline Practice Guideline]". J Urol. 172 (1): 290–294. doi:10.1097/01.ju.0000132159.61156.ea.
  12. Buvat, J.; Tesfaye, F.; Rothman, M.; Rivas, D. A.; Giuliano, F. (2009). "Dapoxetine for the Treatment of Premature Ejaculation: Results from a Randomized, Double-Blind, Placebo-Controlled Phase 3 Trial in 22 Countries". European Urology. 55 (4): 957–968. doi:10.1016/J.Eururo.2009.01.025.
  13. "Éjaculation précoce: pas de dapoxétine" [Premature ejaculation: not dapoxetine]. Prescrire (in French). 29 (313): 811–814. 2009.
  14. McMahon, C. G.; Kim, S. W.; Park, N. C.; Chang, C. P.; Rivas, D.; Tesfaye, F.; Aquilina, J. W. (2010). "Treatment of Premature Ejaculation in the Asia-Pacific Region: Results from a Phase III Double-blind, Parallel-group Study of Dapoxetinejsm_1560256..268". The Journal of Sexual Medicine. 7: 256–268. doi:10.1111/j.1743-6109.2009.01560.x.
  15. Montejo, A. L.; Llorca, G.; Izquierdo, J. A.; Rico-Villademoros, F.; Psychotr, S. W. G. S. (2001). "Incidence of sexual dysfunction associated with antidepressant agents: A prospective multicenter study of 1022 outpatients". The Journal of Clinical Psychiatry. 62: 10–21.
  16. Jhanjee, A.; Kumar, P.; Bhatia, M. S.; Srivastava, S. (2011). "Dapoxetine-A Novel Drug for Premature Ejaculation". Delhi Psychiatry Journal. 14 (1): 5.
  17. Modi, N. B.; Dresser, M.; Desai, D.; Jazrawi, R. P. (2005). "Dapoxetine for the treatment of premature ejaculation: Lack of interaction with ethanol". Journal of Urology. 173 (4): 239–239.
  18. Gengo, P. J.; View, M.; Giuliano, F.; McKenna, K. E.; Chester, A.; Lovenberg, T.; Gupta, S. K. (2005). "Monoaminergic transporter binding and inhibition profile of dapoxetine, a medication for the treatment of premature ejaculation". Journal of Urology. 173 (4): 239–239.
  19. Goldstein, Irwin (17 November 2003). "The Central Mechanisms of Sexual Function". Boston University School of Medicine. Retrieved 11 February 2020.
  20. Giuliano, F.; Clement, P. (2005). "Physiology of ejaculation: emphasis on serotonergic control. [Review]". Eur Urol. 48 (3): 408–417. doi:10.1016/j.eururo.2005.05.017.
  21. Clement, P.; Bernabe, J.; Gengo, P.; Denys, P.; Laurin, M.; Alexandre, L.; Giuliano, F. (2007). "Supraspinal site of action for the inhibition of ejaculatory reflex by dapoxetine". European Urology. 51 (3): 825–832. doi:10.1016/J.Eururo.2006.10.011.
  22. McMahon, C. G.; Althof, S. E.; Kaufman, J. M.; Buvat, J.; Levine, S. B.; Aquilina, J. W.; Porst, H. (2011). "Efficacy and safety of dapoxetine for the treatment of premature ejaculation: integrated analysis of results from five phase 3 trials. [Meta-Analysis Research Support, Non-U.S. Gov't]". J Sex Med. 8 (2): 524–539. doi:10.1111/j.1743-6109.2010.02097.x. PMID 21059176.
  23. Dapoxetine: a guide to its use in premature ejaculation (D. T. Perspective, Trans.). (2011) (Vol. 27, pp. 1-4).
  24. Dresser, M.; Lindert, K.; Lin, D.; Gidwani, S.; Gupta, S. K.; Modi, N. B. (2004). "Pharmacokinetics of single and multiple escalating doses of dapoxetine in healthy volunteers". Clinical Pharmacology & Therapeutics. 75 (2): P32. doi:10.1016/J.Clpt.2003.11.123.
  25. Kowey, P. R.; Mudumbi, R. V.; Aquilina, J. W.; DiBattiste, P. M. (2011). "Cardiovascular safety profile of dapoxetine during the premarketing evaluation. [Research Support, Non-U.S. Gov't]". Drugs in R&D. 11 (1): 1–11. doi:10.2165/11587660-000000000-00000. PMC 3585760. PMID 21410293.
  26. Khan, A.; Khan, S.; Kolts, R.; Brown, W. A. (2003). "Suicide rates in clinical trials of SSRIs, other antidepressants, and placebo: Analysis of FDA reports". American Journal of Psychiatry. 160 (4): 790–792. doi:10.1176/Appi.Ajp.160.4.790. PMID 12668373.
  27. Tamam, L.; Ozpoyraz, N. (2002). "Selective serotonin reuptake inhibitor discontinuation syndrome: A review". Advances in Therapy. 19 (1): 17–26. doi:10.1007/Bf02850015. PMID 12008858.
  28. McMahon, C. G. (2012). "Dapoxetine: a new option in the medical management of premature ejaculation". Ther Adv Urol. 4 (5): 233–251. doi:10.1177/1756287212453866. PMC 3441133. PMID 23024705.
  29. Hellstrom WJ (2009). "Emerging treatments for premature ejaculation: focus on dapoxetine". Neuropsychiatr Dis Treat. 5: 37–46. doi:10.2147/ndt.s3251. PMC 2695237. PMID 19557098.
  30. Owen RT (2009). "Dapoxetine: a novel treatment for premature ejaculation". Drugs Today. 45 (9): 669–78. doi:10.1358/dot.2009.45.9.1388694. PMID 19956808.
  31. Waldinger, M. D. (2007). "Premature ejaculation — Definition and drug treatment". Drugs. 67 (4): 547–568. doi:10.2165/00003495-200767040-00005.
  32. Venkatesan, K., & Srinivasan, K. V. (2008). A stereoselective synthesis of (S)-dapoxetine starting from trans-cinnamyl alcohol. arkivoc, 16, 9.
  33. Dapoxetine: LY 210448. (2005). [Review]. Drugs in R&D, 6(5), 307-311.
  34. Priligy for Premature Ejaculation: Partnership with Menarini. (2012) Retrieved 17 November 2012, from http://www.furiex.com/pipeline/marketed-products/priligy/
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.