EDUCATIONAL LIBRARY
PT-141
Bremelanotide is a melanocortin receptor agonist.
Aliases: bremelanotide, vyleesi
Half-life context
Unknown. Not normalized across research products; see the approved-product pharmacokinetics.
Regulatory status
Checked 2026-10-09
FDA product approval
approved product. Vyleesi (bremelanotide); approval does not extend to research-labeled PT-141 products.
Compounding
not established. Compounded products do not carry FDA product approval; legal eligibility is not established here.
Research status
product specific. Premenopausal women with acquired, generalized hypoactive sexual desire disorder meeting the Vyleesi label.
Sport status
unknown. Not individually verified; consult your sport authority.
Evidence A
Established human clinical or approved-product evidence for the specified indication.
Grades describe the cited population and indication, not safety or suitability for an individual.
Population: Premenopausal women with acquired, generalized hypoactive sexual desire disorder meeting the Vyleesi label.
Indication: Approved labeled indication only.
Basis: Product-label clinical evidence.
Risks
- Blood-pressure increases and nausea are label warnings.
Contraindications
- Uncontrolled hypertension or known cardiovascular disease are labeled contraindications.
Interactions
- Delayed gastric emptying can affect absorption of oral medicines; the label advises avoiding oral naltrexone-containing products and reviewing medicines requiring threshold concentrations.
What to record
- Existing clinician-directed records, symptoms and dated health measurements.
- Record missing data; trends do not demonstrate causation.
A licensed clinician must interpret the evidence for your situation. This entry provides education, not treatment instructions.
Review: source-curated; clinician review pending
Sources
- Primary evidence or regulator source. Checked 2026-10-09
Where to buy
Optional partner links, separate from the research above.
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