MC4R agonism in hypothalamus activates sexual arousal pathways. Unlike PDE5 inhibitors, acts centrally on CNS rather than peripherally on vasculature.
Studies have administered: 1.25–1.75mg SC in FDA-approved study ranges
RECONNECT trials: Statistically significant improvement in satisfying sexual events and desire in HSDD. Female sexual arousal studies show CNS-mediated arousal independent of hormonal status.
Nausea (40% in trials), flushing, blood pressure transient increase, hyperpigmentation with repeated use documented
These compounds have been examined together in research literature. Combination use is not endorsed or recommended — this information is provided for research context only.
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