Most medicines for sexual problems act on blood flow. PT-141 works differently: it acts on signalling pathways in the brain that are linked to desire. Developed under the name bremelanotide, it became a US prescription medicine for women in 2019, sold as Vyleesi. Here you can read what it is, what the studies found and where it stands in Europe.
PT-141 began with a surprise. In the early 1990s, researchers testing an experimental tanning peptide noticed that some male volunteers had an unexpected side effect: spontaneous erections. A small US company, Palatin Technologies, set out to keep that effect and leave the tanning behind. The result was PT-141, a short peptide folded into a ring.
Instead of widening blood vessels like the well-known erection pills, it switches on melanocortin receptors in the brain. These receptors help control appetite, skin colour and sexual motivation. That is why it was tested both in men with erectile problems and in women with low desire.
Its road to the pharmacy was long. A nasal spray was dropped in 2008 because it raised blood pressure, and an injection won US approval in 2019 for premenopausal women whose low sexual desire causes distress. The pages below explain each step.
| What it is | A synthetic, ring-shaped peptide of seven amino acids, related to the body's own hormone alpha-MSH |
| Other names | Bremelanotide and bremelanotide acetate; brand name Vyleesi |
| Molar mass | About 1,025 g/mol |
| Target | Melanocortin receptors in the brain, above all the MC4 receptor |
| Approved use | In the US only: premenopausal women with acquired, generalised hypoactive sexual desire disorder (HSDD) |
| Market history | Developed by Palatin Technologies; FDA approval in June 2019; sold to Cosette Pharmaceuticals in 2023 |
| Status | No marketing authorisation in the EU or the UK |
Nothing here is medical advice, and research-grade PT-141 is not intended for people. If you have concerns about desire, arousal or your sex life, a doctor is the right person to talk to.