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PT-141 (Bremelanotide)_Dosage, benefits & legal status

Also known as bremelanotide, Vyleesi, PT141

Published July 22, 2026 · Updated July 25, 2026

An approved shot that boosts sexual desire through the brain.

LibidoMelanocortin agonistFDA-approved
Common vial size10 mg
Dose1.75 mg per dose
FrequencyAs needed, before activity
RouteUnder the skin (subcutaneous)
StatusFDA-approved
CycledNot cycled, but the label caps it: one dose in 24 hours, and no more than 8 in a month

Common vial size is what vendors typically sell, not a recommendation. Enter your own vial in the calculator.

See how this dose compares across the library →

01

What is PT-141 (Bremelanotide)?

Plain language first. The technical label stays, but it never stands alone.

Overview

It raises sexual desire through brain signaling rather than blood flow, which is different from how erection drugs work. It is FDA-approved for low libido in women.

The technical version

PT-141 (bremelanotide) is a melanocortin receptor agonist, a cyclic peptide that acts on the MC4R receptor in the brain.

What it's used for

An approved shot that boosts sexual desire and arousal by acting on the brain rather than blood flow. It is used for low libido in both women and men.

02

How does PT-141 (Bremelanotide) work?

What it does in the body, and where.

PT-141 works on the brain rather than on blood flow, which makes it fundamentally different from the erectile-dysfunction drugs it gets compared to.

  1. 01
    It activates MC4R in the brain
    A melanocortin receptor involved in sexual desire, appetite, and arousal signaling.
  2. 02
    Desire rises, rather than blood flow
    Drugs like sildenafil act on blood vessels. This acts upstream of that, on the wanting rather than the mechanics.
  3. 03
    Approved for one specific group
    FDA-approved as Vyleesi for low sexual desire in premenopausal women. Use in men is off-label and less studied.
Anatomical illustration highlighting brain
WHERE THIS COMPOUND IS THOUGHT TO ACT:
Brain

03

What else is it used for?

Each group carries its own evidence level.

Approved means regulators have cleared it for that purpose. Investigational means it is in trials. Early research means it is being studied and is not established.

Sexual desire in women

FDA-approved
  • RegulatoryApproved by the FDA in June 2019 for low sexual desire that causes distress in premenopausal women.
  • Human trialTwo late-stage trials in more than 1,200 women showed improved desire and reduced distress against placebo, though the effect was modest.
  • Human trialNausea affected 40% of users, particularly with the first injection. It required anti-nausea treatment in 13% and caused 8% to stop.

Sexual function in men

Investigational
  • Human trialIn men who did not respond to standard erection drugs, about 34% responded against 9% on placebo.
  • No dataCompounded versions are not the approved product and have not been reviewed by the FDA.
Study

The approved use is in women, and the male findings come from smaller off-label studies we could not link to a primary source.

The published record

Research index

135

Papers and trials about PT-141 (Bremelanotide)

Searched: PT-141, bremelanotide, Vyleesi, PT141.

91 papers tagged human · 38 not reviews or lab · 16 clinical trial publications

10 registered trials · 4 with posted results

Furthest stage reached: Approved in the US

Compare this against the whole library →

In animals23
In the lab1
Reviews54
Senior author shareSpread across many groups

Evidence summary

Counted from Europe PMC indexing, not read by a person; a human tag can land on reviews, commentary or lab papers; clinical trial publications is the narrower count.

PT-141 (Bremelanotide) vial rendering
Compound field notes

At a glance

Four things to know about PT-141 (Bremelanotide)

01

Evidence

FDA-approved

02

Category

Sexual and hormonal

03

Common vial

10 mg

04

Half-life

About 2.7 hours

04

How much, and do you cycle it?

The range, and whether you take breaks.

1.75 mg per dose, as needed, before activity. Not cycled, but the label caps it: one dose in 24 hours, and no more than 8 in a month FDA label

Taken as needed rather than on a schedule, but the label sets a hard ceiling on frequency because of transient blood pressure rises and skin darkening with repeat dosing. That ceiling is the closest thing to a cycling rule here, and it is a real one.

Source: VYLEESI (bremelanotide) FDA label

Compare this against the whole library →

05

How long does it stay in the body?

The half-life, and where the figure comes from.

About 2.7 hoursFDA label

Largely cleared from plasma within 12 hours, which is why the label sets a 24 hour minimum between doses.

Source: Vyleesi (bremelanotide) label section 12.3

You can compare this against the whole library to see where it sits.

06

How do I dose and price it?

Enter your vial and your dose. Pick a mix. We show the draw and the cost.

The vial holds a fixed amount of drug. Adding more water does not make more drug, it just spreads it thinner, so you draw a bigger number on the syringe for the same dose.

Your vial size (mg)
Printed on the vial.
What you paid per vial
$
Used for cost per dose only.
Your dose (mg)
Commonly referenced dose: 1.75 mgFDA label

Choose your mix

your own mL
units · —
Enter your own volume

Measuring the water1 mL = one full 100-unit syringe.

YOUR DRAW35 / 100 units
What it costs

PT-141 (Bremelanotide) starts at $19.24 across 164 vendors, typically $2.87 – $7.00 per mg.

216 listings, last read Oct 24, 2026. Shipping and card fees are not included.

See all 216 listings →
07

How do you store it?

Before mixing, and after.

Follow the label that came with it.

This is an approved product, and its own label sets how long it keeps once mixed. Those windows vary enormously between products, from use-immediately to about a month, so the label is the only thing worth following here. Vials of the same compound sold by peptide vendors arrive with no label and no established holding time.

08

What are the side effects and cautions?

Known cautions and warnings for this compound.

Solubility, computed: 71% charged residues, 43% hydrophobic. Water usually sufficient.

A first-pass rule from peptide manufacturers' guidance. It does not account for disulfide bridges, salt form or how the powder was dried, and it predicts what should be easy rather than what will happen in your vial.

Who should avoid it

Check these before anything else.
  • Uncontrolled high blood pressure
  • Known cardiovascular disease
  • Pregnancy

Stop and get help

These are emergencies. Seek care.
  • Chest pain or a severe headache with a racing heart
  • An erection lasting more than four hours, which is a medical emergency
  • Signs of an allergic reaction

Common effects

Expected, and usually mild.
  • Nausea, which is the most common effect
  • A temporary rise in blood pressure and drop in heart rate
  • Flushing and headache
  • Darkening of skin or gums with repeated use

Where this page says nothing is established, that means nobody has studied it, not that a compound is safe.

09

Is PT-141 (Bremelanotide) approved?

And where the numbers on this page come from.

Yes. PT-141 (Bremelanotide) is FDA approved and available on prescription in the United States.

  • Approval status
    FDA-approved
  • Route
    Under the skin (subcutaneous)
  • Checked
    22 July 2026
  • Dose
    From the drug label. The manufacturer tested this range and a regulator reviewed it.
  • Vial size
    From what vendors typically list; not a recommendation.
  • Sources

What has happened recently

FDA-approved in June 2019 as Vyleesi for acquired, generalised hypoactive sexual desire disorder in premenopausal women. The label sets limits the research market does not: no more than one dose in 24 hours and no more than eight doses a month, both to limit blood pressure effects. It is contraindicated in uncontrolled high blood pressure or known cardiovascular disease, and the label states it is not indicated for postmenopausal women, for men, or to enhance sexual performance.

What regulators say

From official documents

Enforcement naming this compound

  • Vendor product named as an unapproved new drug (Royal Peptides, August 2026)

    The vendor's product, not the approved Vyleesi This is a finding about one seller's vial, not about the compound or any approved product containing it.

    Read the letter

Guides for this compound

Sources

Beyond these, 135 records are indexed. Browse the records