FDA-approved drug
PT-141 is a real approval with modest numbers. We print both, then show you what the vials leave out.
Bremelanotide (Vyleesi) earned a genuine FDA approval in 2019 for low sexual desire in premenopausal women: desire scores rose 0.30 to 0.42 points more than placebo on a 1.2-to-6.0 scale, distress improved, and satisfying sexual events did not significantly change. The same label counts 40% nausea and a possibly permanent skin-darkening risk. Meanwhile the gray market sells 'PT-141' vials to men for performance, the exact uses the label rules out, on small 2004-to-2008 trials, two of which now carry journal integrity flags. Every number on this site links to its source.
- 1FDA-approved use, and we quote its exact boundary
- 38fetch-verified sources, every one peer-reviewed or government
- 15studies in the graded evidence table, species labeled on every row
- 2male-use trials in that table carry journal integrity flags, and the rows say so
Online care, from intake to delivery
Bremelanotide care, made simple
Choose your plan, complete a private medical intake, and connect with a licensed provider. If prescribed, treatment ships discreetly to your door.

Your care plan includes
Everything you need to get started
Encrypted checkout • provider review required • shipping included
- 01Choose your planSelect the supply and refill preference that works for you.
- 02Complete your intakeShare your health history in our private, secure flow.
- 03Provider reviewIf appropriate, your prescription is prepared and shipped.
Prescription treatment requires an online medical evaluation. A provider will determine whether treatment is medically appropriate; approval is not guaranteed.
Key facts
- StatusFDA-approved drug
- SC bioavailability~100%
- Volume of distribution25.0 L (mean)
- Clearance6.5 L/hr (CL/F)
- Protein binding21%
- Dose plateauCmax plateaus at 7.5 mg SC (~4.3x approved dose)
- Excretion64.8% urine, 22.8% feces (radiolabel)
- ClassMelanocortin receptor agonist (cyclic heptapeptide alpha-MSH analog)
- Approved useAcquired, generalized HSDD in premenopausal women
- Explicitly not indicatedMen; postmenopausal women; enhancing sexual performance
- Dose1.75 mg SC autoinjector, at least 45 min before activity
- Half-lifeAbout 2.7 h (range 1.9 to 4.0)
- TmaxAbout 1.0 h (range 0.5 to 1.0)
- Desire effect vs placebo+0.30 and +0.42 points (scale 1.2 to 6.0); integrated +0.35
- Satisfying sexual eventsNo significant change vs placebo in either phase 3 trial
- Nausea rate40.0% vs 1.3% placebo
- Key contraindicationUncontrolled hypertension or known cardiovascular disease
- MoleculeC50H68N14O10, MW 1025.2 (free base), PubChem CID 9941379
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Practical calculators and references, each scoped and sourced.
All guides
54 in-depth, individually cited guides.
Dosing 13 guides
Sourcing 13 guides
Evidence 13 guides
Safety 9 guides
Comparisons 6 guides
Get the real-numbers brief before you believe a vial pitch
One email: the exact phase 3 numbers including the null endpoint, the label limits, the nausea and pigmentation odds, and the autoinjector-vs-vial difference. Cited, No dosing advice by email. Unsubscribe anytime.
