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BETA

PT-141 (Bremelanotide)

PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide melanocortin receptor agonist developed from Melanotan II, acting on MC1R, MC3R, and MC4R to produce centrally mediated sexual arousal rather than acting peripherally on vascular tissue as PDE5 inhibitors do. It received FDA approval in 2019 (Vyleesi) for hypoactive sexual desire disorder (HSDD) in premenopausal women, making it the first approved melanocortin-based pharmaceutical for sexual dysfunction. Unlike sildenafil or tadalafil, PT-141 is effective regardless of genital blood flow and shows some evidence of benefit in men with erectile dysfunction non-responsive to PDE5 inhibitors, though this indication is not FDA-approved. It is administered subcutaneously approximately 45 minutes before anticipated sexual activity; common side effects include transient nausea, facial flushing, and blood pressure changes.

peptidesexual healthlibidomoodarousal

Evidence last reviewed: 19 Apr 2026

Research / clinical compound

Not a routine supplement — not recommended for self-directed use.

Information here is educational only, not a recommendation to use. See our Safety page.

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Evidence
4 records
4 recordsBest grade:High

Evidence is from research or clinical settings — does not imply safety outside supervised contexts.

The evidence supports PT-141's effectiveness in increasing sexual desire and satisfaction in premenopausal women with HSDD. However, there are concerns about higher rates of adverse events leading to study discontinuation, indicating a need for careful monitoring.

Safety profile
Premenopausal women with hypoactive sexual desire disorder · Systematic review
High

The most common adverse events were nausea, flushing, headache, and injection site reactions.

Dose in study: 1 mg(trial dose)Duration: Up to 18 months
Adverse event-induced study discontinuation
Premenopausal women with hypoactive sexual desire disorder · Meta-analysis
Moderate

Adverse event-induced study discontinuation was significantly higher in the bremelanotide group compared to placebo.

Dose in study: 1 mg(trial dose)
Sexual satisfaction
Premenopausal women with hypoactive sexual desire disorder · RCT
High

Bremelanotide improved sexual satisfaction and related distress in premenopausal women.

Dose in study: 1 mg(trial dose)Duration: 24 weeksForm: Subcutaneous InjectionTiming: As needed
Sexual desire
Premenopausal women with hypoactive sexual desire disorder · RCT
High

Bremelanotide significantly increased sexual desire and reduced distress related to low sexual desire compared to placebo.

Dose in study: 1 mg(trial dose)Duration: 24 weeksForm: Subcutaneous InjectionTiming: As needed
Stacks containing PT-141 (Bremelanotide)
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This compound is not included in any public supplement stacks.
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Forms & usage
Subcutaneous Injection
Administered as needed, typically 1.75 mg per dose.
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