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For research and educational purposes only. Not intended for human consumption.

PT-141

Extensively Studied
Updated Dec 2025

Bremelanotide | Melanocortin Receptor Agonist

InjectableNasal
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1.75mg
As needed
Injectable
Abdomen (2 inches from navel) or upper thigh
No cycling required
Typical duration
2-8°C
Refrigerated

Overview

What is PT-141?

PT-141 (Bremelanotide) is an FDA-approved synthetic peptide that acts as a melanocortin receptor agonist, specifically targeting MC3R and MC4R receptors in the central nervous system. Unlike traditional ED medications that work through vascular mechanisms, PT-141 directly influences sexual arousal pathways in the brain through dopamine release, making it effective for both male and female sexual dysfunction. A Phase 2 clinical trial (2024) is evaluating bremelanotide co-administered with PDE5 inhibitors for ED treatment in non-responders.

Key Benefits

FDA-approved route with predictable absorption, works within 45 minutes, effective for both male and female sexual dysfunction. Brain-focused mechanism differentiates it from PDE5 inhibitors, showing promise for psychological or central components of sexual dysfunction.

Mechanism of Action

Binds to melanocortin receptors (MC3R/MC4R) in the hypothalamus, mimicking α-MSH to trigger dopamine release, enhancing sexual arousal, desire, and erectile signals via central nervous system pathways rather than direct vascular effects. Effects start ~30-60 minutes post-subcutaneous injection.

Molecular Information

1,025.19 Da
Weight
7
amino acids
Melanocortin receptor agonist
Type
Amino Acid Sequence:
Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
* Cyclic peptide structure for enhanced receptor binding

Pharmacokinetics

Peak
1 hr
Half-life
2.7 hrs
Cleared
~13.5 hrs
100%50%0%0h6h12h18h24h
Peak
Half-life
Cleared
FDA Vyleesi Label

Research Indications

Hypoactive Sexual Desire Disorder (HSDD)

FDA-approved for premenopausal women with acquired, generalized HSDD.

Erectile Dysfunction

Effective in men including those unresponsive to PDE5 inhibitors.

Female Sexual Arousal Disorder

Improves physiological and subjective arousal measures.

Research Protocols

Disclaimer: PT-141 is FDA-approved (as Vyleesi) for HSDD in premenopausal women. These protocols are for research purposes. Consult a healthcare provider before use.

GoalDoseFrequencyRoute
Female HSDD (FDA-approved)1.75mgAs needed, max 1 dose/24hrSubcutaneous
Male Erectile Dysfunction1-2mgAs needed, 45-60min before activitySubcutaneous
Female Arousal Disorder0.75-1.25mgAs needed, max 1 dose/24hrSubcutaneous
Low Starting Dose0.5mgTest dose to assess toleranceSubcutaneous

Timing: Best taken 45-60 minutes before sexual activity. Can be taken with or without food, though food may reduce nausea. Effects last 6-12 hours.

Peptide Interactions

How to Reconstitute

Important: Always use bacteriostatic water (BAC). Sterile technique is essential.

1

Allow vial to reach room temperature (15-20 minutes)

2

Clean vial tops with alcohol swabs

3

Draw 1-2mL bacteriostatic water (1mL for higher concentration)

4

Inject BAC water slowly down the side of PT-141 vial

5

Gently swirl (do not shake) until fully dissolved

6

Solution should be clear and colorless

7

Store reconstituted solution in refrigerator

8

Use within 30 days of reconstitution

Dosing Calculator

Calculate your injection volume with visual dosing guide

FINAL CONCENTRATION
2.50mg/mL
Each milliliter contains 2.50 mg of peptide
VISUAL REFERENCE (RESEARCH USE ONLY)

To obtain 250 mcg from this solution:

Draw 0.10 mL=10 units

(1 mL = 100 units on any insulin syringe)

0102030405060708090100
00.10.20.30.40.50.60.70.80.91.0
0.10 mL
10 units

Draw to this mark for 250 mcg

This calculator is for research purposes only. Always verify calculations and consult protocols.

Quality Indicators

FDA-Approved Pharmaceutical Grade

If prescribed as Vyleesi, guaranteed pharmaceutical quality and safety.

White Crystalline Powder

Pure PT-141 appears as white to off-white lyophilized powder.

Clear Solution When Reconstituted

Properly manufactured PT-141 dissolves completely without cloudiness.

Colored or Oily Appearance

May indicate impurities or degradation - do not use.

Compounded Versions

Ensure compounding pharmacy is licensed and follows USP standards.

What to Expect

  • First 30-45 minutes: May experience mild nausea or facial flushing
  • 45-90 minutes: Onset of effects - increased arousal and desire
  • 2-4 hours: Peak effects - enhanced sexual response
  • 6-12 hours: Effects gradually diminish
  • Long-term: No tolerance development reported with intermittent use

Side Effects & Safety

Side Effects

  • Common side effects: nausea (40%), flushing (20%), headache (11%)
  • Take anti-nausea medication 30 minutes before if prone to nausea
  • Monitor blood pressure - can cause transient decrease
  • Not for use with uncontrolled hypertension or cardiovascular disease
  • Avoid alcohol to minimize blood pressure effects
  • FDA black box warning for blood pressure effects

When to Stop

  • Severe or persistent nausea/vomiting
  • Significant blood pressure changes
  • Allergic reactions
  • Chest pain or shortness of breath
  • Consult healthcare provider immediately

References

4 Studies

Phase 2 Trial: Bremelanotide + PDE5i (2024)

Human | ~50 men | Open-label dose-escalation | PDE5i non-responders (30-40% of ED patients)

FDA-cleared Phase 2 trial evaluating subcutaneous bremelanotide co-administered with PDE5 inhibitors in men who don't respond to traditional ED medications. Topline results expected end of 2024, with potential Phase 3 in early 2025 - the first new class in ~20 years.

FDA Approval Trial for HSDD

Human | 1.75mg subcutaneous | As needed | 24.5% improvement vs 17.2% placebo

Phase 3 trials in premenopausal women with HSDD showed statistically significant improvements in sexual desire and reduced distress, leading to FDA approval as Vyleesi.

Male Erectile Dysfunction Double-Blind Trial

Human | Bremelanotide vs placebo | NCT01382719 | Statistically significant ED improvements

Double-blind clinical study reported statistically significant erectile function improvements versus placebo, supporting efficacy in male sexual dysfunction.

Quick Start Guide

Typical Dose
1.75mg for women, 1-2mg for men
How Often
As needed, 45-60 minutes before activity
Where to Inject
Abdomen (2 inches from navel) or upper thigh
Timing
45-60 minutes before anticipated sexual activity
Effects Timeline
Onset 45-60min, peak 2-4 hours, duration 6-12 hours
Storage
Refrigerate reconstituted solution 2-8°C
Cycle Length
No cycling needed - use as required
Break Between
Minimum 24 hours between doses

Research Disclaimer

PT-141 is sold for laboratory research purposes only and is not intended for human or animal consumption. The information provided on this page is compiled from published research, veterinary studies, and anecdotal reports for educational purposes. This content does not constitute medical advice, diagnosis, or treatment recommendations. Any research involving PT-141 must comply with all applicable local, state, and federal regulations. BioInfinity Lab makes no claims regarding the safety or efficacy of PT-141 for any purpose. Consult qualified professionals for any research applications.