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0269881107078490v1
22/1/55    most recent
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First published on August 22, 2007, doi:10.1177/0269881107078490

Journal of Psychopharmacology 2008;22:55.

A more recent version of this article appeared on January 1, 2008


Article

Selective serotonin re-uptake inhibitor treatment-emergent sexual dysfunction: randomized double-blind placebo-controlled parallel-group fixed-dose study of a potential adjuvant compound, VML-670

David S. Baldwin1*, John Hutchinson2, Kirsteen Donaldson2, Bob Shaw3, and Andrew Smithers4

1 Clinical Neuroscience Division, University of Southampton, Southampton, UK
2 Vernalis Ltd, Oakdene Court, Winnersh, Reading, UK
3 Vernalis Ltd, Oakdene Court, Winnersh, Reading, UK.
4 Profiad Ltd, Reading, UK

* To whom correspondence should be addressed.


   Abstract

Sexual dysfunction is common during acute and continuation treatment of depressed patients with selective serotonin (5-hydroxytryptamine, 5-HT) re-uptake inhibitors (SSRIs), but there is no consensus on clinical management. Compounds with 5-HT1A agonist properties have been proposed as adjuvant agents in patients continuing with SSRIs. Randomized double-blind placebo-controlled parallel-group fixed-dose 4-week treatment study. Previously depressed male or female patients in symptomatic remission receiving stable doses of fluoxetine or paroxetine but experiencing treatment-emergent sexual dysfunction were randomised to double-blind treatment with placebo or VML-670 (a 5-HT1A and 5-HT1D agonist). Sexual dysfunction was assessed by the Arizona Sexual Experiences Scale (ASEX). Two-hundred and eighty-eight patients (204 women, 84 men; mean age 44.2 years) received VML-670 (n=149; 107 women, 42 men) or placebo (n=139; 97 women, 42 men). In the intention-to-treat, last-observation carried forward analysis (n=282), proportionately more patients became free of sexual dysfunction with VML-670 (34.3% versus 27.9% with placebo) but this difference was not statistically significant. Male patients treated with VML-670 showed a significantly greater (p=0.01) improvement in ability to achieve and maintain penile erection (a secondary outcome measure). A similar proportion of patients reported on-treatment, treatment-emergent adverse events with VML-670 (71.1%) and placebo (68.3%), and a similar proportion experienced at least one treatment-related adverse event (36.9% versus 35.3%). Double-blind treatment with VML-670 offered no significant advantage over placebo on the primary outcome measure in the overall sample. Further studies may be warranted in larger groups of male patients with sexual dysfunction.

Key Words: SSRI, sexual dysfunction, placebo-controlled study, 5-HT1A agonist


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