Compound Reference Overview
| Field | Value |
|---|---|
| Name | PT-141 (Bremelanotide) |
| Reference Code | PT-141 |
| Category | Sexual Health / Melanocortin Receptor Agonist |
| Example Strength | 10 mg vial (varies by formulation) |
| Reference Range | 0.5–2 mg as needed (FDA-approved dose: 1.75 mg) |
| Frequency | As needed, ≥45 minutes before activity (not more than once in 24 hours) |
| Key Safety Warning | FDA limits to 8 doses per month. Nausea is common (~40%). May cause temporary skin hyperpigmentation and blood pressure changes. |
Mechanism of Action (Educational)
PT-141 (Bremelanotide) is a melanocortin receptor agonist, primarily targeting MC4 receptors within the central nervous system.
Unlike PDE5 inhibitors, PT-141 acts centrally rather than peripherally. It increases sexual desire and arousal by modulating dopaminergic pathways involved in sexual motivation.
Indications (Regulatory / Off-Label)
- FDA-approved: Hypoactive Sexual Desire Disorder (HSDD) in premenopausal women (Vyleesi)
- Off-label: Erectile dysfunction
- Off-label: Low libido (men and women)
Administration (Clinical Use)
| Parameter | Details |
|---|---|
| Route | Subcutaneous |
| Frequency | As needed |
| Injection Sites | Abdomen or thigh |
| Timing | 45 minutes to 2 hours before sexual activity |
Titration Schedule (Clinical Framework)
- Week 1: 0.5–1 mg test dose
- Week 2+: 1–2 mg as needed
- FDA-approved dose: 1.75 mg
- Maximum: 1 dose per 24 hours, 8 doses per month
Start low due to nausea risk. Pre-treatment with anti-emetic may be considered.
Pharmacokinetics (Literature)
- Onset: 45 minutes to 2 hours
- Half-life: ~2–3 hours
- Peak response varies by individual
Reconstitution & Concentration (Mathematical Illustration Only)
| Parameter | Value |
|---|---|
| Diluent | Bacteriostatic water (example only) |
| Reconstitution Volume | 2 mL (example) |
| Resulting Concentration | 5 mg/mL (5000 mcg/mL) |
| Stability | Up to 28 days refrigerated (varies by formulation) |
Reconstitution Math Example
- 10 mg ÷ 2 mL = 5 mg/mL
- 0.1 mL = 0.5 mg
- 0.2 mL = 1.0 mg
- 0.35 mL = 1.75 mg (FDA dose)
Provided strictly for arithmetic reference.
Mathematical Calculation Tool
The calculator below allows concentration and volume calculations based on vial strength and dilution volume. This tool is provided strictly for mathematical reference.
Peptide Reconstitution Calculator
For Educational & Professional Reference Only
Safety & Contraindications (Summary)
Contraindications
- Uncontrolled hypertension
- Cardiovascular disease
- Pregnancy or breastfeeding
- Concurrent use of naltrexone
Drug Interactions
- Naltrexone (high): significantly reduces efficacy
- Antihypertensives (moderate): additive blood pressure effects
Adverse Events
- Nausea (~40%)
- Flushing
- Headache
- Injection site reactions
- Skin hyperpigmentation
Serious Risks
- Transient blood pressure elevation
- Focal hyperpigmentation
Monitoring (Clinical Framework)
- Blood pressure
- Nausea severity
- Skin changes
Disclaimer
Bremelanotide (Vyleesi) is FDA-approved for HSDD in premenopausal women. Other uses are off-label. This content is provided strictly for educational and professional reference purposes. All clinical decisions must be made by a licensed healthcare professional.
Reference Sources
1. Kingsberg SA, et al. Bremelanotide for HSDD in premenopausal women.
Obstet Gynecol. 2019.
2. Clayton AH, et al. Safety and efficacy of Bremelanotide.
J Sex Med. 2019.