
PT-141 (bremelanotide) is a cyclic melanocortin receptor agonist that works centrally in the brain to enhance sexual desire and arousal. Unlike PDE5 inhibitors that work peripherally on blood flow, PT-141 targets the melanocortin system in the hypothalamus.
Research-context information only. PT-141 is the active ingredient in an FDA-approved product for women's hypoactive sexual desire disorder; off-label and research-peptide forms for other uses are not FDA-approved. Protocols, doses, and reactions reported below come from published clinical trials and self-reported community sources. This article reports what has been documented, not what should be done. Consult a licensed physician for personal medical decisions.
PT-141 is FDA-approved for women with HSDD at 1.75 mg. Community protocols use lower doses (500 mcg) to balance efficacy with tolerability. This is not medical advice.
PT-141 (Bremelanotide) Dosing Table
Match your vial size below — reconstitution and dose math update automatically.
| Dose | Syringe units | mL volume | Schedule |
|---|---|---|---|
| 500 mcg | 10 units | 0.1 mL | On-demand SubQ (45-90 min before)Starter |
| 1 mg | 20 units | 0.2 mL | On-demand SubQStandard |
| 1.75 mg | 35 units | 0.35 mL | On-demand SubQVyleesi clinical dose |
Math assumes U-100 insulin syringes (1 mL = 100 units). Verify your syringe matches before injecting. Round half-units to the nearest visible mark.
Quick Reference: Standard Protocol
| Parameter | Detail |
|---|---|
| Vial | 10 mg |
| BAC Water | 2 mL |
| Concentration | 5 mg/mL (5,000 mcg/mL) |
| Dose | 500 mcg (10 units on insulin syringe) |
| Route | Subcutaneous |
| Timing | 30 minutes before activity |
| Frequency | As needed (max once per 24 hours) |
| Cycle | As needed |
| Storage | Refrigerate, use within 28 days |
Cycling Details
PT-141 is an on-demand medication — no loading phase, no fixed cycling. Use as needed, maximum once per 24 hours.
First-time use: Community protocols describe a 500 mcg starting dose to assess tolerability. Nausea is commonly reported on initial doses but typically decreases with repeated use.
Tolerance management: Some users report decreased effectiveness with frequent use. Taking 1-2 weeks off every month may help maintain sensitivity.
Timing optimization: Effects begin 15-30 minutes post-injection and peak at 1-2 hours. Community sources describe injecting 30 minutes before anticipated activity.
Routes of Administration
Subcutaneous injection is the only practical route. Clinical trials and the FDA-approved formulation both use SC injection.
- Injection sites: Abdomen, thigh, upper arm — anywhere with subcutaneous fat
- Volume: 0.1 mL with an insulin syringe (29-31 gauge)
- Not oral: PT-141 is a cyclic peptide degraded by stomach acid
- Not nasal: Early research explored nasal delivery, but SC proved more reliable

Reconstitution Quick Reference
| Vial Size | BAC Water | Concentration | 500 mcg Dose | 1 mg Dose |
|---|---|---|---|---|
| 10 mg | 2 mL | 5 mg/mL | 10 units | 20 units |
Math: 10 mg / 2 mL = 5 mg/mL = 5,000 mcg/mL. For 500 mcg: 500 / 5,000 = 0.1 mL = 10 units.
Community protocols describe gentle swirling — not shaking — to avoid degrading the peptide, with storage at 2–8°C and use within 28 days.




