PT-141 (Bremelanotide)
FDA-approved for female sexual arousal disorder
Aperçu
PT-141 (Bremelanotide) is a melanocortin receptor agonist approved by the FDA for treatment of hypoactive sexual desire disorder (HSDD) in premenopausal women.
Key Information
Mechanism
Activates melanocortin receptors in the brain, specifically MC4R, to increase sexual desire independently of the vascular system.
Benefits
- Increased sexual desire
- FDA-approved for HSDD
- Brain-mediated (not vascular)
- On-demand use
Side Effects
- Nausea (40%)
- Flushing
- Headache
- Skin darkening
Contraindications
- Cardiovascular disease
- Pregnancy
Evidence Summary
FDA-approved based on Phase 3 trials for hypoactive sexual desire disorder.
Research
FDA-approved as Vyleesi based on Phase 3 trials showing significant improvement in sexual desire and distress.
View ResearchSafety
FDA-approved. Side effects: nausea, flushing, headache.
Legal Status
FDA-approved as Vyleesi for female HSDD.
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S'inscrireRating Breakdown
Avis
PT-141 (bremelanotide) restored my libido completely. The fact it's FDA-approved for HSDD is a major plus. Brain-mediated mechanism is different from vascular drugs - works on desire not just blood flow. On-demand use is convenient.
PT-141 takes about 2 hours to kick in. The desire increase is real - not just physical. Nausea is the main side effect. FDA approval makes me feel safe. Better than PDE5 inhibitors for psychological ED.