Bremelanotide Rx

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.

Bremelanotide care catalog product image
Compounded injectable treatmentPrepared after approval
Catalog image. Dispensed product and packaging may vary by pharmacy.

Your care plan includes

Everything you need to get started

From$153per month
Licensed providerMedical reviewIf prescribedTreatment includedAt no added costDiscreet shippingWhen you need itOrder support
Choose your planChange or cancel future refills anytime
Due today$170.10then monthly

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  1. 01
    Choose your planSelect the supply and refill preference that works for you.
  2. 02
    Complete your intakeShare your health history in our private, secure flow.
  3. 03
    Provider 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%source
  • Volume of distribution25.0 L (mean)source
  • Clearance6.5 L/hr (CL/F)source
  • Protein binding21%source
  • Dose plateauCmax plateaus at 7.5 mg SC (~4.3x approved dose)source
  • Excretion64.8% urine, 22.8% feces (radiolabel)source
  • ClassMelanocortin receptor agonist (cyclic heptapeptide alpha-MSH analog)FDA labelsource
  • Approved useAcquired, generalized HSDD in premenopausal womenFDA labelsource
  • Explicitly not indicatedMen; postmenopausal women; enhancing sexual performanceFDA labelsource
  • Dose1.75 mg SC autoinjector, at least 45 min before activityFDA labelsource
  • Half-lifeAbout 2.7 h (range 1.9 to 4.0)FDA labelsource
  • TmaxAbout 1.0 h (range 0.5 to 1.0)FDA labelsource
  • Desire effect vs placebo+0.30 and +0.42 points (scale 1.2 to 6.0); integrated +0.35Human RCTsource
  • Satisfying sexual eventsNo significant change vs placebo in either phase 3 trialFDA labelsource
  • Nausea rate40.0% vs 1.3% placeboFDA labelsource
  • Key contraindicationUncontrolled hypertension or known cardiovascular diseaseFDA labelsource
  • MoleculeC50H68N14O10, MW 1025.2 (free base), PubChem CID 9941379Chemical referencesource

Read the full Bremelanotide monograph

Browse by topic

Everything on PT-141 (bremelanotide), organized the way you research it.

All guides

54 in-depth, individually cited guides.

Dosing 13 guides

Sourcing 13 guides

Evidence 13 guides

Safety 9 guides

Comparisons 6 guides

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