FDA Approved (Vyleesi)SubQ · Central Acting

PT-141

Bremelanotide — Melanocortin Receptor Agonist

Half-life
~2.7 hours
Route
SubQ
Typical dose
1.25–2 mg SubQ
Reconstitutable
Yes

What is PT-141?

PT-141 (Bremelanotide) is a synthetic melanocortin peptide acting centrally on MC3R and MC4R receptors to increase sexual desire and arousal. It is the first FDA-approved non-hormonal treatment for hypoactive sexual desire disorder (HSDD) in premenopausal women, marketed as Vyleesi.

Unlike PDE5 inhibitors which work peripherally through vascular mechanisms, PT-141 acts centrally in the hypothalamus and limbic system to increase dopamine activity and sexual motivation — making it effective for both men and women, including cases where psychological or neurological factors contribute.

Research Evidence

GoldFemale HSDD

Phase 3 trials supporting FDA approval demonstrated significant improvement in satisfying sexual events and desire scores vs placebo in premenopausal women with HSDD.

SilverMale Erectile Dysfunction

Phase 2 trials showed dose-dependent improvements in erectile response, including in patients who did not respond to PDE5 inhibitors.

Evidence grades: Gold = RCT human data · Silver = multiple animal studies, consistent · Bronze = limited or preliminary

Dosing Protocols

Standard dose
1.25–2 mg SubQ
Start at 1.25mg to assess tolerance. FDA-approved dose for women is 1.75mg. Community protocols use 1-2mg for men.
Timing
45–60 min before activity
Takes 45-60 minutes to reach peak CNS effect. Effects can last 6-12 hours.
Frequency
Max 1x per 24 hours
FDA labeling recommends no more than once per 24 hours.

Reconstitution Guide

Vial SizeBAC WaterConcentrationTarget draw
2 mg1 ml2 mg/ml1mg = 50 units
10 mg5 ml2 mg/ml1mg = 50 units
Calculate your exact protocol →

Frequently Asked Questions

Does PT-141 work for men?

Yes. Though FDA-approved only for women, PT-141 has Phase 2 clinical trial data in men showing significant improvements in erectile function, including in men who did not respond to PDE5 inhibitors. It works centrally through dopaminergic activation rather than peripheral vascular effects.

What are the main side effects of PT-141?

Flushing (transient facial redness and warmth) occurs in 40-60% of users. Nausea is the second most common effect, particularly at higher doses. Both typically peak 30-90 minutes post-injection and resolve within a few hours.

References

  1. [1]Diamond LE, Earle DC, Heiman JR, et al. An effect on the subjective sexual response in premenopausal women with sexual arousal disorder by bremelanotide (PT-141). J Sex Med. 2006;3(4):628-638.
  2. [2]U.S. Food & Drug Administration. Vyleesi (bremelanotide) prescribing information. AMAG Pharmaceuticals. 2019.
Disclaimer: This profile is for informational and research purposes only. Not medical advice. Always consult a licensed healthcare provider before using any compound.

This profile was prepared using AI-assisted research synthesis. Citations are provided where applicable — verify with primary sources before clinical application.

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