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Evidence: A✓ FDA-approvedSexual Health

PT-141: Benefits, Dosage & FDA Status

Bremelanotide (Vyleesi)

A melanocortin receptor agonist that works directly on the nervous system to increase sexual desire. The only FDA-approved peptide for sexual dysfunction that acts on the brain rather than vascular system.

FDA Status

FDA-approved for hypoactive sexual desire disorder (HSDD) in women

Typical Dose

1.75 mg subcutaneous, 45 min before activity

Evidence Grade

AStrong RCT or FDA-approved evidence

Half-Life

~2.7 hours

Routes of Administration

subcutaneous

First Synthesized

2003

Clinics Indexed

210 providers have offered PT-141 in our tracked directory.

Mechanism of Action

Cyclic 7-amino-acid melanocortin receptor agonist (primarily MC4R) that activates dopaminergic pathways governing sexual desire.

Key Reported Benefits

Benefits listed reflect commonly reported effects from clinical trials and practitioner use. Individual response varies. Evidence-grade A indicates strong rct or fda-approved evidence.

Reported Side Effects

  • Nausea
  • Flushing
  • Headache
  • Transient blood-pressure rise

Contraindications

  • Uncontrolled hypertension
  • Cardiovascular disease
  • Pregnancy

Regulatory & Safety Context

FDA status: FDA-approved for hypoactive sexual desire disorder (HSDD) in women

This page is for educational purposes only and does not constitute medical advice. Peptide use outside of an FDA-approved indication should be discussed with a licensed medical professional. Source quality, cold-chain storage, and injection hygiene all materially affect safety outcomes.

See state-by-state legality: US peptide legality by state →

References

Selected primary literature on PT-141. Full PubMed records linked. Additional citations are available on request.

  1. PubMed PMID 31166290
  2. PubMed PMID 30939066

Last reviewed: 2026-04-30

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