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PT-141
Also known as: Bremelanotide / Vyleesi
FDA-Approved
Bremelanotide is a melanocortin receptor agonist (MC4R-preferring) approved for HSDD in premenopausal women.
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Overview
Bremelanotide is a melanocortin receptor agonist (MC4R-preferring) approved for HSDD in premenopausal women.
FDA Approval Status
Approved by the FDA for at least one medical indication (see approved uses below).
Mechanism of Action
Central melanocortin receptor agonism.
Current Research
RECONNECT trials.
Research strength: Strong
Potential Medical Uses
- Acquired, generalized HSDD in premenopausal women
Potential Benefits
- On-demand dosing
Known Side Effects
- Nausea
- Flushing
- Injection-site reactions
- Transient BP elevation
Contraindications
- Uncontrolled hypertension
- Cardiovascular disease
Drug Interactions
- Oral naltrexone (reduced efficacy)
Administration Methods
- Subcutaneous autoinjector
Half-life
~2.7 hours
Reconstitution
Prefilled autoinjector.
Storage & Handling
Room temperature per label.
References & Sources
Frequently Asked Questions
Information on this page is educational and general in nature. It is not medical advice. Consult a qualified healthcare professional before making any medical decisions.