Mood & Libido · Rx only

PT-141, prescribed — not just shipped.

Skip the gray-market guesswork. A licensed clinician reviews your health history, a licensed U.S. pharmacy compounds your prescription, and a care team stays with you after it ships.

$243 / mo$270 as a single month · $648 for a 3-month supply

A licensed clinician reviews every request. If PT-141 fits your health history, they write your prescription and your pharmacy takes it from there.

Licensed U.S. providers Licensed U.S. pharmacy All 50 states + D.C.

Requires an online medical evaluation. Prescribed only when a licensed provider determines it's appropriate.

A licensed clinician in a consultation room
PT-141 vial and spec card
PT-141 · Rx only
1

Share your health history

PT-141 has its own online clinical questionnaire — your history, medications, and goals.

2

Your answers get a careful review

A clinician reads your history and takes the time to get it right before anything is prescribed.

3

Your pharmacy ships

Compounded for your prescription and shipped cold-chain, with care-team check-ins after.

The safe way to take PT-141 seriously

PT-141 is easy to find online and hard to trust there. Promise works the way medicine is supposed to work — a clinician decides, a licensed pharmacy fills, and someone stays accountable to you.

A real prescription

Prescribed for you specifically, after a real look at your health history — never pulled off a shelf.

A real pharmacy

Your prescription is compounded for you by a licensed U.S. pharmacy — not a mystery vial from an unregulated website.

Real oversight

Temperature-safe shipping, follow-up check-ins, and a care team that answers — before and after your medication arrives.

Product details
Form
Injectable vial (subcutaneous), 2 mg per mL
Supply
28-day supply
Pharmacy
Compounded by a licensed U.S. pharmacy
Availability
Ships to all 50 states + D.C.; not all treatments are available in every state

Acts on melanocortin receptors

PT-141 is an analog of alpha-melanocyte-stimulating hormone, studied at the MC4R receptor rather than on the vascular pathway familiar from oral medications.

Central pathways, not blood flow

The research interest sits in brain circuits associated with sexual desire — a different question from the mechanics that PDE5 inhibitors address.

Prescribed, never simply supplied

A licensed provider reviews your history, including blood pressure and cardiovascular background.

In brief.

Most of what people know about treating sexual function comes from one family of medicines that works on blood flow. PT-141 is studied somewhere else entirely: the central nervous system pathways involved in desire itself. That distinction is the reason it exists as a separate conversation, and it is the most useful thing to understand before a visit.

PT-141, also called bremelanotide, is a synthetic melanocortin receptor agonist. Promise offers it one way only — a licensed provider reviews your health history and prescribes it only when treatment is appropriate for you.

What PT-141 is

PT-141 is a small synthetic peptide, an analog of alpha-melanocyte-stimulating hormone, the signaling molecule the body uses at the melanocortin receptors. It arrived at this category sideways. The molecule came out of research on a tanning compound, and the sexual-response signal investigators kept noticing in that work became the reason it was developed on its own.

The receptor that matters most in the published research is MC4R, which is expressed in the brain, including in the hypothalamus. That is a different address from where the familiar oral medications act, and it is why PT-141 sits in our mood and libido category rather than anywhere vascular.

Central signaling, not blood flow

Medications in the PDE5 inhibitor class — sildenafil, tadalafil and their relatives — act on peripheral blood vessels. They work through the nitric oxide pathway in vascular smooth muscle and change what happens locally, which is why their effect depends on arousal already being present.

PT-141 is studied at the other end of that sequence. The research interest is in melanocortin signaling inside central circuits associated with sexual desire, not in vessel dilation. In practical terms the two lines of research address different questions: one is about mechanics, one is about interest.

Which question applies to a given person — or whether the honest answer is neither, and something else is going on, from sleep to thyroid to a medication already in the cabinet — is a clinical judgment. It is not something to settle from a product page.

Where the evidence stands

Bremelanotide is not FDA-approved in compounded form; the one FDA-approved bremelanotide product is indicated for one narrow use: acquired, generalized hypoactive sexual desire disorder in premenopausal women. That is the extent of the approval. The compounded PT-141 prescribed through Promise is not FDA-approved, and compounded medications are not reviewed by the FDA for safety, effectiveness, or quality.

The trial literature behind that approval is the strongest human data the compound has, and it is worth reading plainly. The reported effects were modest. Nausea was the most commonly reported adverse event, with flushing and headache close behind, and transient changes in blood pressure and heart rate have been described. Repeated dosing has been associated with skin darkening in some people, an expected consequence of acting on melanocortin receptors.

None of that is a reason to be squeamish about the compound. It is a reason it goes through a prescriber.

How PT-141 is prescribed

The intake questionnaire for PT-141 is its own clinical form, not a generic one. It covers your health history, your current medications, your blood pressure and cardiovascular background, and what you are actually trying to address. A licensed provider reads it.

If PT-141 fits your history, they write the prescription and set the protocol. Not everyone qualifies, and in this category particularly, declining is often the correct clinical answer — low desire has many causes, and several of them are addressed by fixing something else first.

What treatment looks like

If you are prescribed, your medication is compounded and dispensed by a licensed U.S. pharmacy, and shipped in discreet, temperature-safe packaging. Dosing and timing come from your provider's protocol rather than from a chart found online; the distance between a reasonable dose and an unpleasant one is one of the reasons this is a prescription at all.

After that it is follow-up. Your care team checks in, and anything that needs adjusting gets adjusted with a clinician involved. If you want to understand the other compound studied in this category, kisspeptin approaches the same territory from upstream, through the hormone axis rather than through central melanocortin signaling.

Common questions

What is PT-141?

PT-141, also called bremelanotide, is a small synthetic peptide and an analog of alpha-melanocyte-stimulating hormone. It acts as an agonist at melanocortin receptors, and the receptor most discussed in the research is MC4R, which is expressed in the brain. That is what makes it unusual in this category: the studied mechanism is central signaling rather than peripheral blood flow.

How is PT-141 different from medications like sildenafil or tadalafil?

They are studied at opposite ends of the same sequence. Sildenafil and tadalafil are PDE5 inhibitors that act on the nitric oxide pathway in peripheral blood vessels, which is why their effect depends on arousal already being present. PT-141 is studied for melanocortin signaling in central circuits associated with desire itself. One line of research addresses mechanics, the other addresses interest, and which of those applies to a given person is a clinical question rather than a self-diagnosis.

Is PT-141 FDA-approved?

Not in the form offered here. An FDA-approved bremelanotide product exists, indicated only for acquired, generalized hypoactive sexual desire disorder in premenopausal women. The compounded PT-141 prescribed through Promise is not FDA-approved, and compounded medications are not reviewed by the FDA for safety, effectiveness, or quality. It is prepared by a licensed U.S. compounding pharmacy against a prescription written for you specifically.

Do I need a prescription, and how does the visit work?

Yes, and every request goes through a clinician. You complete the intake questionnaire built for PT-141, which is its own clinical form covering your health history, medications, cardiovascular background, and what you are trying to address. A licensed provider reviews your answers and prescribes only when PT-141 is appropriate for you. If you are prescribed, a licensed U.S. pharmacy compounds and dispenses your medication and ships it in temperature-safe packaging.

What side effects have been reported in the research?

Nausea is the most commonly reported adverse event in the bremelanotide trial literature, along with flushing and headache. Transient increases in blood pressure and reductions in heart rate have been described, and repeated dosing has been associated with darkening of the skin in some people, which is an expected consequence of acting on melanocortin receptors. Your provider weighs these against your history, which is a large part of why this compound is prescribed.

Related treatments

Other Mood & Libido options a provider may consider.