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PT-141 (Bremelanotide)
Sexual Wellness

PT-141 (Bremelanotide)

FDA-approved for women with low sexual desire.

PT-141 (bremelanotide) is FDA-approved only for premenopausal women with hypoactive sexual desire disorder, marketed as Vyleesi since 2019. Use for other purposes is off-label and not FDA-approved.

Injectable vial2 mg/mL (5 mL vial)

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PT-141 (Bremelanotide) Monthly Plan$170 billed monthly
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How it works

How PT-141 (Bremelanotide) works

PT-141, the compound name for bremelanotide, operates through a fundamentally different pathway than PDE5 inhibitors such as sildenafil or tadalafil. As an alpha-MSH analog, it binds melanocortin receptors in the hypothalamus, engaging central dopamine and oxytocin signaling associated with sexual desire and arousal, rather than acting on vascular tissue. Arousal cues remain necessary for the medication to have an effect; PT-141 does not work through vasodilation.

What to expect

Timeline & results

Standard administration is injection approximately 45 minutes prior to anticipated activity, with onset occurring 45 to 90 minutes post-injection and a duration of action lasting 4 to 8 hours. Efficacy data comes from the RECONNECT-1 and RECONNECT-2 trials, where roughly 40% of participants reported meaningful improvement in desire, compared with approximately 20% on placebo.

Getting started

Care that fits your life

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Key benefits

What PT-141 (Bremelanotide) is used for

The only medication FDA-approved for hypoactive sexual desire disorder in premenopausal women.

Acts on melanocortin receptors in the hypothalamus, a central desire pathway distinct from vascular mechanisms.

Demonstrated meaningful improvement in roughly 40% of RECONNECT trial participants, compared with about 20% on placebo.

Designed to complement PDE5 inhibitors rather than replace them, since the two act through separate pathways.

Safety information

Important safety information

PT-141 is FDA-approved only for premenopausal women with hypoactive sexual desire disorder. Use for other purposes is off-label and not FDA-approved. Blood pressure that isn't well controlled rules PT-141 out entirely, as does a documented hypersensitivity reaction to bremelanotide. Providers weigh cardiovascular disease, impaired liver or kidney function, and any prior history of malignancy with added caution. Nausea affects roughly 40% of users, most often within the first 2 hours of injection and diminishing with subsequent doses. Additional reported effects include headache, injection-site reactions, a temporary elevation in blood pressure, and flushing, along with hyperpigmentation, darkening of the skin or existing moles, with repeated use. Because the melanocortin pathway has a theoretical association with melanoma, patients should report any new or changing moles to their provider. This product is compounded by a licensed pharmacy and is not FDA-approved. It has not undergone FDA review for safety or efficacy.

This page is educational and is not medical advice. Tell your provider about your full medical history and current medications before starting treatment.

About

About PT-141 (Bremelanotide)

PT-141, also known by its chemical name bremelanotide, is a synthetic cyclic heptapeptide derived from the naturally occurring alpha-melanocyte-stimulating hormone (alpha-MSH). It acts as an agonist at melanocortin receptors, particularly MC3R and MC4R, which are expressed in areas of the brain involved in sexual function, including the hypothalamus and limbic system. Unlike many other treatments for sexual dysfunction, PT-141 works centrally -- through the nervous system -- rather than through vascular mechanisms, which distinguishes its pharmacological profile from agents like sildenafil or tadalafil.

PT-141 is typically administered as a subcutaneous injection 45 minutes to 2 hours before anticipated sexual activity. Dosing is individualized and determined by a licensed provider following a clinical review. The peptide's effects have been reported to begin within one to two hours and may persist for several hours. Because it does not rely on vascular signaling, it has been studied in both men and women, including those who have not responded to other approaches to sexual dysfunction.

In clinical study programs, participants reported subjective improvements in sexual desire, arousal, and overall sexual experience. The FDA approved a nasal spray formulation of bremelanotide (Vyleesi) for hypoactive sexual desire disorder (HSDD) in premenopausal women in 2019, which provides context for the established regulatory and clinical understanding of this compound. Compounded injectable PT-141 is prepared at 503A pharmacies for patients whose licensed providers determine it appropriate after a clinical evaluation.

PT-141 is generally considered a fit for adults who have undergone a clinical assessment for sexual dysfunction and are seeking an option that works through central desire pathways. It may be relevant for individuals who have not found success with other modalities, or for whom vascular-acting agents are not appropriate. As with all compounded peptides dispensed at FormBlends, PT-141 is only provided after a licensed provider reviews your online visit and determines it clinically appropriate.

Common side effects reported in clinical studies include transient nausea, flushing, and headache, typically mild and resolving within hours. Blood pressure monitoring is a relevant safety consideration, as transient increases in blood pressure have been observed. PT-141 is not appropriate for patients with cardiovascular conditions including uncontrolled hypertension, or for those taking antihypertensive medications, without provider guidance. A thorough health history review during your online visit will identify any contraindications.

FAQ

Frequently asked questions

Is PT-141 approved for men?+

No, PT-141 is FDA-approved only for premenopausal women with hypoactive sexual desire disorder. Use for other purposes, including in men, is off-label and not FDA-approved. Any use outside the approved population should be discussed carefully with a provider, since the safety and efficacy data was generated specifically in women with HSDD.

How is PT-141 different from Viagra?+

PT-141 and Viagra work through completely different mechanisms. Viagra (sildenafil) is a PDE5 inhibitor that increases blood flow, while PT-141 acts on melanocortin receptors in the brain to engage pathways involved in sexual desire, not blood flow. PT-141 still requires arousal cues to have an effect, and it's FDA-approved for a different population: premenopausal women with HSDD.

Does PT-141 cause nausea?+

Yes, nausea is the most common side effect of PT-141, reported by about 40% of users in clinical trials. It typically occurs within the first 2 hours after injection and tends to lessen with repeated doses. Other reported effects include flushing, injection-site reactions, headache, and a temporary rise in blood pressure.

How long does PT-141 last?+

PT-141 is typically injected about 45 minutes before anticipated activity, with onset generally occurring within 45 to 90 minutes. Its effects last roughly 4 to 8 hours. Because it works through a central desire pathway rather than blood flow, timing is less about a single moment and more about the window it stays active.

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