Sildenafil, tadalafil and the rest are PDE5 inhibitors. They act on the body’s physical response.
They help the body follow through once desire is already there. They do not create the wanting.
A peptide that works on desire and arousal, the spark that comes before the moment.
Pay only if approved.
Less than $5 a day.* One price, one peptide, no membership fee stacked on top.
*Based on the 12-month plan. Subject to provider approval.
Here is what almost nobody explains. Desire and erection are two different systems. Blood-flow medications act on the second one. They help the body follow through on a signal that has already been sent. If the signal itself never arrives, there is nothing for them to work with. That signal is a brain event, and it runs through a set of receptors most people have never heard of.
Most of this category treats the last step. PT-141 is studied on the first one.
Sildenafil, tadalafil and the rest are PDE5 inhibitors. They act on the body’s physical response.
They help the body follow through once desire is already there. They do not create the wanting.
Bremelanotide is a melanocortin receptor agonist. It acts centrally, in the brain, not on blood vessels.
It is studied on the desire and arousal signalling that comes before the physical response.
Compounded PT-141 is not FDA-approved. Onset and duration vary from person to person. A licensed provider decides whether PT-141 is appropriate for you, and approval is not guaranteed.
Bremelanotide is a melanocortin receptor agonist that acts on the central nervous system. This is a different mechanism from PDE5 inhibitors, which work on blood flow.
Molinoff et al, Ann N Y Acad SciThe FDA approved bremelanotide as Vyleesi in 2019 for acquired, generalized hypoactive sexual desire disorder in premenopausal women. That is its only approved indication. Prescribing it to men is off-label.
FDA approval, 2019The Phase 3 evidence comes from the two RECONNECT trials, conducted in premenopausal women with acquired, generalized HSDD.
Kingsberg et al, Obstet Gynecol 2019 (PMID 31599840)In the 52-week open-label extension, the most common adverse events were nausea in 40.4% of participants, flushing in 20.6% and headache in 12.0%. Nausea was usually transient. We would rather you read that here than find it later.
Simon et al, Obstet Gynecol 2019 (PMID 31599847)Published research on bremelanotide is not research on this compounded product, and results in a trial population are not a prediction of your result. Individual results vary and are not guaranteed.
A five-minute intake, online, in your own words. No waiting room and no appointment to book.
A US-licensed provider reads your history and decides whether PT-141 is appropriate for you. Approval is not guaranteed.
Shipped free from a licensed US compounding pharmacy. Nothing on the box says what is inside.
Message your care team any time. Dose changes and questions cost nothing extra.
Every plan includes the full telos rx care experience. A licensed provider reviews your intake first. If you are not approved, or PT-141 is not right for you, you pay nothing.
A licensed provider reviews your intake before anything ships. If you are not approved, you pay nothing.

The reason most people come looking. PT-141 is studied on the brain signalling behind desire and arousal, not on the physical response further down the chain.

If blood-flow medications did not help, that is information. PT-141 acts through a different pathway, which is exactly why people who have already tried the usual options look at it.

People describe feeling more emotionally present with their partner rather than managing a performance. That is a described experience, not a promised outcome.

Taken only when you choose, which is a very different relationship than a pill you take every day whether or not the evening goes anywhere.
Descriptions of patient experience come from published clinical literature, not from telos rx patient data. PT-141 does not work for everyone and individual results vary.
Five minutes online. A US-licensed provider reviews your intake and decides whether PT-141 is appropriate for you, and approval is not guaranteed. Approved, and it ships free in plain packaging. As low as $138 per month.
Compounded PT-141 is not FDA-approved and has not been evaluated by the FDA for safety, effectiveness or quality. Bremelanotide is FDA-approved as Vyleesi for acquired, generalized hypoactive sexual desire disorder in premenopausal women only; that is its sole approved indication, and any other use, including use in men, is off-label and determined by a licensed provider. PT-141 is available only by prescription and is subject to medical approval by a licensed provider based on your online intake. Approval is not guaranteed. This is an asynchronous online telehealth service and is not a substitute for in-person or emergency care.
Common side effects may include nausea, flushing, headache, fatigue, injection-site reactions and a temporary increase in blood pressure. Focal darkening of the skin has been reported with repeated dosing. Do not use PT-141 if you have uncontrolled high blood pressure or known cardiovascular disease. Tell your provider about all medications you take, including naltrexone and PDE5 inhibitors. Seek medical attention if you experience a severe or persistent reaction.
PT-141 is not intended to diagnose, treat, cure or prevent any disease. Published research on bremelanotide was conducted on the approved product, not on this compounded preparation, and trial results are not a prediction of your result. Individual results vary and are not guaranteed. Testimonials reflect one individual’s experience and are not typical or a guarantee of results. Availability and formulations may vary by state. Prices shown are current as of publication and subject to change.