MC4R agonist in the central nervous system associated with sexual desire and arousal, with clinical data in HSDD and earlier work in erectile dysfunction.
View medication pageSexual Health
Sexual health therapies in this hub are organized around desire, arousal, and central nervous system signaling. These compounds belong here because the clinical and mechanistic literature links melanocortin or oxytocin pathways to sexual desire, arousal, bonding, or aspects of sexual function, although the quality and consistency of evidence differ across products and populations.
Available Medications
Each medication below is grouped here because its mechanism, clinical use, or published literature helps explain why it fits this therapy category.
Studied for effects on desire, arousal, lubrication, bonding, and sexual satisfaction, though findings are mixed across settings.
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Contact us for moreStudies, data, and supporting evidence
These references support the positioning statements used on this therapy hub. They are intended as educational source material for patients and prescribers, not as a substitute for individualized medical judgment.
The phase 3 RECONNECT trials showed bremelanotide improved sexual desire and reduced related distress in premenopausal women with HSDD.
Full Text →NAMS supports low-dose vaginal estrogen as an effective option for moderate to severe GSM, including dyspareunia and vaginal dryness, when nonprescription measures are insufficient.
PubMed →This phase 3 trial found vaginal estradiol improved dyspareunia, vaginal pH, and epithelial markers, supporting local estradiol therapy for GSM-related sexual discomfort.
PubMed →The consensus concludes that the only evidence-based indication for testosterone in women is HSDD, which supports careful sexual-health positioning while avoiding broader unsupported claims.
Full Text →ISSWSH offers detailed clinical guidance for systemic testosterone therapy in women with HSDD, including monitoring and use within physiologic ranges.
PubMed →