PT-141 (Bremelanotide)
Research indicates this melanocortin receptor agonist may influence sexual function and metabolic parameters.
Human Trials
8
2,847 participants
Risk Level
Monthly Cost
Varies by source and frequency of use
Quick Facts
- Category
- Pharmaceutical
- Research Field
- Pharmacology
- Evidence Grade
- B- – Promising
- Risk Level
- Medium
- Monthly Cost
- $200 – $800
- Human Trials
- 8
Typical Dose
0.75–2 mg intranasally, as needed
Range
0.5–2 mg per dose
For informational purposes only – not medical advice. See disclaimer
Research Velocity
Mechanism of Action
PT-141 (bremelanotide) is a synthetic melanocortin receptor agonist that primarily targets MC4R and MC1R receptors in the central nervous system. Studies suggest it activates hypothalamic pathways involved in sexual arousal and appetite regulation. Research indicates the compound may influence dopaminergic and noradrenergic signaling, potentially affecting both sexual function and metabolic processes through central melanocortin system activation.
Overview
PT-141 (bremelanotide) is a synthetic peptide that research indicates acts as a melanocortin receptor agonist, primarily targeting MC4R receptors in the hypothalamus. Originally developed from the tanning peptide Melanotan II, studies suggest PT-141 influences sexual arousal through central nervous system pathways rather than vascular mechanisms. The FDA approved it in 2019 as Vyleesi for treating hypoactive sexual desire disorder in premenopausal women, administered via subcutaneous injection.
Clinical trials indicate that PT-141 may increase sexual desire and arousal through activation of melanocortin pathways in the brain. Research suggests the compound works by stimulating dopaminergic and noradrenergic signaling in areas associated with sexual motivation. Beyond its approved indication, some studies explore its potential metabolic effects, as melanocortin receptors play roles in energy homeostasis and appetite regulation.
Research indicates common side effects include nausea, flushing, and injection site reactions, with some studies noting transient increases in blood pressure and heart rate. The compound requires subcutaneous injection and is typically used on an as-needed basis rather than daily dosing. While approved for a specific indication in women, off-label research and use in other populations continues, though long-term safety data remains limited.
Known Interactions
- May interact with medications affecting blood pressure due to potential hypotensive effects
- Possible interactions with other melanocortin system modulators
- Potential additive effects with other centrally-acting compounds affecting sexual function
Legal Status by Country
Your country (United States)
FDA-approved as Vyleesi for hypoactive sexual desire disorder
Available without prescription in:
India, Mexico, Panama
📍 = your selected country · ✈️ = medical tourism destination · Always verify current local regulations before travel.
Key Research
- 2019
Primary efficacy data from pivotal trials
- 2018
Phase 2 efficacy and safety data
- 2020Melanocortin-4 receptor agonists for the treatment of obesity
Mechanistic background on MC4R pathway
- 2021Central melanocortin system and energy homeostasis
Metabolic effects of melanocortin activation
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Last verified: 2026-03-16