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Intrinsic Longevity
Sexual & relational wellness

PT-141

Also known as: Bremelanotide

A prescription medicine, sold as Vyleesi, that works on arousal signals in the brain instead of on blood flow.

Class
Melanocortin medicine
Drug name
Bremelanotide (Vyleesi)
Approved for
Premenopausal women
FDA status
FDA-approved (one use)
Overview

What it is

PT-141 is the research name for bremelanotide, sold as Vyleesi. It switches on melanocortin receptors in the brain, so it works on desire signals rather than on blood flow to the genitals.

PT-141 has an unusual origin. It came out of research on melanotan 2, a tanning compound, when researchers noticed an unexpected effect on arousal and followed that thread instead.

It was approved in 2019 under the name Vyleesi for one situation: premenopausal women with acquired, general low sexual desire that causes them real distress.

The label is unusually specific about what it is not for. It states plainly that it is not approved for women past menopause, not approved for men, and not approved to improve sexual performance.

Benefits

What it supports

  • FDA-approved for premenopausal women with low sexual desire that causes them distress
  • Works through brain arousal signals, so it fits a different situation than blood-flow medicines
  • Gives providers an option to weigh when a blood-flow medicine is not the right match
  • Any use outside the approved group is off-label and is a provider's call
Mechanism

How it works

1

Most sexual-wellness medicines work on blood flow. PT-141 does not.

2

It switches on melanocortin receptors in the brain, in regions involved in desire and arousal. The signal starts in the nervous system rather than in blood vessels.

3

That is why it is described as working on wanting rather than on the physical response. It addresses a different part of the picture than a blood-flow medicine does.

4

It is used as needed before activity rather than every day. The same receptor family explains its side effects, including nausea and darker patches of skin.

Context

Who it's for

Premenopausal women with low sexual desire that troubles them, discussing the approved use with a provider

People trying to understand the difference between desire and physical response

Adults comparing a brain-acting option with blood-flow medicines like tadalafil

Anyone sorting out how PT-141 relates to melanotan 2, since the two share a starting point

Landscape

In the landscape

How this therapy compares to related options—not a recommendation.

  • Melanotan 2

    The compound PT-141 came from. It reaches more receptors, has never been approved, and carries serious safety concerns.

  • Tadalafil

    Works on blood flow rather than on brain signals, so it addresses a different part of the picture. Both sit in the sexual & relational wellness area of the library.

  • Oxytocin Acetate

    Tied to closeness and calm rather than desire signals or blood flow. Another pathway in the same sexual-wellness area.

Provider-directed

What providers review

  • Your sexual health history and what specifically feels different
  • Blood pressure and heart health, since it briefly raises blood pressure
  • Medicines you take now, including anything else for sexual wellness
  • How well you tolerate nausea, which is the most common side effect
  • Mood, relationship context, and other causes worth ruling out first

For therapies that require medical evaluation, every protocol is designed by a licensed provider.

Suitability for PT-141 is determined by a licensed provider after evaluation.

Questions

PT-141 FAQ

Good to know

Regulatory & considerations

Bremelanotide (PT-141) is FDA-approved for one specific use: premenopausal women with acquired, general low sexual desire that causes distress. Its label states it is not approved for women past menopause, not approved for men, and not approved to boost sexual performance. Any other use is off-label and is decided by a licensed provider.

Therapies that require medical evaluation are sourced from FDA-regulated 503A compounding pharmacies.

For therapies that require medical evaluation, every protocol is designed by a licensed provider.

The approval covers premenopausal women only. Use by men or by women past menopause is off-label and is a provider's decision.

Nausea is common, affecting a large share of people in the trials, and it is usually worst with the first dose.

It raises blood pressure briefly after each dose, so it is not used by people with uncontrolled high blood pressure or known heart disease.

A small number of people develop darker patches of skin on the face, gums, or breasts, and that darkening does not always fade.

Shop PT-141

See current pricing and availability for PT-141 in our shop. If a medical evaluation is needed, a licensed provider guides you through it.

Individual results vary. General information on this site is not a substitute for professional medical advice.