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Hormonal

PT-141 (Bremelanotide)

Research indicates this melanocortin receptor agonist may influence sexual function and metabolic parameters.

Human Trials

8

2,847 participants

Risk Level

Medium Risk

Monthly Cost

$200$800 /month

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

Timing45–90 min before desired effect
Formintranasal spray (bremelanotide; compounded prescription)
NotesPrescription only in most jurisdictions. FDA-approved as Vyleesi for hypoactive sexual desire disorder in women. Side effects: nausea (dose-dependent), transient blood pressure increase, flushing. Do not use more than once every 24 hours.

For informational purposes only – not medical advice. See disclaimer

Research Velocity

+50%
12 publications in the last 12 months · major increase in publications

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

Rx Required
✈️

Available without prescription in:

India, Mexico, Panama

✈️India
Unregulated
✈️Mexico
Unregulated
✈️Panama
Unregulated
📍United States
Rx Required
Australia
Restricted
✈️Brazil
Restricted
Canada
Restricted
✈️Colombia
Restricted
Germany
Restricted
✈️Israel
Restricted
Netherlands
Restricted
Switzerland
Restricted
✈️Thailand
Restricted
✈️Turkey
Restricted
✈️UAE
Restricted
United Kingdom
Restricted
China
Banned
Japan
Banned
Russia
Banned
✈️South Korea
Banned

📍 = your selected country · ✈️ = medical tourism destination · Always verify current local regulations before travel.

Key Research

Where to Source·Prescription required – consult your healthcare provider

Last verified: 2026-03-16