
FDA Approval of Bremelanotide for Female Sexual Desire Disorder Changes Market
Hypoactive sexual desire disorder is currently the most common form of sexual dysfunction among women in the US. There's also limited treatment options for it.
The new approval for bremelanotide injection (Vyleesi) serves as an unprecedented embrace to US marketing for female sexual dysfunction therapy.
Last week, the US Food and Drug Administration (FDA) approved bremelanotide as the first product indicated for premenopausal
HSDD is currently the most common form of sexual dysfunction among women in the US. It’s characterized by reduced sexual desire and distress not attributed to any other medical, pharmacologic, psychiatric, or even relationship-based issues.
When the therapy reaches the market—as anticipated, in September of this year—it will be available for a patient population which market research indicates up to 95% of all afflicted premenopausal women are unaware of. According to Palatin, approximately 6 million women meet the diagnostic criteria for generalized HSDD.
“This is reflected in the biopharmaceutical industry, if you look at Viagra and its overwhelming success and the numerous other drugs for male erection that have been marketed successfully,” Sophocles said at the time. “There is only one FDA approved medication that relates to or whose purpose is to enhance the female sexual experience.”
Sophocles noted that common sexual dysfunction symptoms in women include physical manifestations—painful intercourse, pelvic pain, endometriosis, muscle dysfunction—as much as they include psychiatric issues—depression, lowered self-esteemed, and burdens on relationships.
She agreed with the notion that sexual dysfunction has been perceived as a taboo topic among most afflicted women. She estimated
“So there is a little bit of a, ‘Don't ask, don't tell’ problem,” Sophocles said. “Women are, to use a cliched term, suffering in silence. They're not talking about it, they often feel it's just them, there's something wrong with them, they're broken.”
The current mechanism of action executed by bremelanotide is unknown, but investigators believe the therapy functions by binding to the central nervous system’s melanocortin receptors—a region associated with sexual function.








































































