PT-141 Dosage: Doses Studied, Units and Chart
What doses of PT-141 have been used in published research, how they convert to syringe units, and what is still unknown.
- Doses studied
- 9 studies
- with a stated dose, listed below
- Frequency
- Varies by study
- as used in studies
- Half-life
- approximately 2.7 hours (range 1.9-4.0 h)
- subcutaneous, in people · FDA label (Vyleesi)
- Vial sizes sold
- 10 mg
Dosing on the FDA label
Quoted from the approved product label. It applies to the approved product used as prescribed, not to compounded or research-chemical versions.
- 1.75 mg subcutaneously, as needed, at least 45 minutes before anticipated sexual activity · FDA label (Vyleesi)
- Not more than one dose within 24 hours; no more than 8 doses per month · FDA label (Vyleesi)
- Dose cap per month · FDA label (Vyleesi)
Doses used in published studies
Each dose below is quoted from a study abstract, strongest design first. Animal doses are labelled and do not translate directly to people. None of them is a recommendation.
| Dose | Frequency and route | Study type | Source |
|---|---|---|---|
| 1.75 mg | as needed before sexual activity · subcutaneous · 24 weeks | Human RCTn = 1202 | Journal of women's health 2022, PMID 35230162 |
| 1.75 mg | as needed · subcutaneous · 24 weeks | Human RCTn = 1267 | Obstetrics and gynecology 2019, PMID 31599840 |
| 1.75 mg | subcutaneous | Human RCT | The journal of sexual medicine 2019, PMID 31277966 |
| 0.75, 1.25 and 1.75 mg | subcutaneous | Human RCTn = 397 | Journal of hypertension 2017, PMID 27977473 |
| 20 mg | single doses on days 1, 4 and 7, with or without ethanol · intranasal | Human RCTn = 24 | Clinical therapeutics 2017, PMID 28189361 |
| 0.75, 1.25 or 1.75 mg | as desired · subcutaneous · 12 weeks | Human RCTn = 327 | Women's health 2016, PMID 27181790 |
| 10 mg | 45 minutes to 2 hours before sexual stimulation, at least 16 doses/attempts · intranasal | Human RCTn = 342 | The Journal of urology 2008, PMID 18206919 |
| 20 mg | single dose · intranasal | Human RCTn = 18 | The journal of sexual medicine 2006, PMID 16839319 |
| 0.3 to 10 mg healthy; 4 or 6 mg in ED patients | subcutaneous | Human RCT | International journal of impotence research 2004, PMID 14999221 |
Dose to syringe units
For a 10 mg vial mixed with 2 mL of bacteriostatic water (5 mg/mL), on a U-100 syringe. These are reference amounts for the math, not suggested doses.
- 0.25 mg
- 5 u
- 0.5 mg
- 10 u
- 1 mg
- 20 u
- 1.5 mg
- 30 u
- 2 mg
- 40 u
- 2.5 mg
- 50 u
Before anyone considers it
- PT-141 is FDA approved for HSDD (Vyleesi); research-chemical versions are not the approved drug.
- Compounded and research-chemical versions are not the approved product and are not checked by the FDA for identity, purity or dose.
- Reconstitution math (mg vs mcg, units vs mL) is the most asked question in peptide forums. Check every number twice.
- People who are pregnant, breastfeeding, or have a chronic condition need medical advice first.
Common questions
How many units is 1 mg of PT-141?
It depends on the water added. A 10 mg vial with 2 mL of water gives 5 mg/mL, so 1 mg is 20 units on a U-100 syringe. Use the calculator for other mixes.
Is PT-141 FDA approved?
PT-141 is FDA approved for HSDD (Vyleesi). Products sold as research chemicals are not the approved drug and are not checked by the FDA.
More on PT-141
Sources
- 1Metric (SI) Prefixes (NIST Reference on Constants, Units, and Uncertainty)National Institute of Standards and Technology (NIST) · 2025physics.nist.govAccessed 2 Oct 2026
- 2BASAGLAR (insulin glargine) injection, prescribing information (DailyMed)U.S. Food and Drug Administration / DailyMed (Eli Lilly and Company label) · 2026dailymed.nlm.nih.govAccessed 2 Oct 2026
- 3These highlights do not include all the information needed to use VYLEESI ® safely and effectively. See full prescribing information for VYLEESI VYLEESI (bremelanotide injection), for subcutaneous use Initial U.S. Approval: 2019FDA label (Vyleesi), DailyMed · current labeldailymed.nlm.nih.govAccessed 2 Oct 2026
- 4Prespecified and Integrated Subgroup Analyses from the RECONNECT Phase 3 Studies of Bremelanotide.Journal of women's health (2002) · 2022PMID 35230162Accessed 2 Oct 2026
- 5Bremelanotide for the Treatment of Hypoactive Sexual Desire Disorder: Two Randomized Phase 3 Trials.Obstetrics and gynecology · 2019PMID 31599840Accessed 2 Oct 2026
- 6Responder Analyses from a Phase 2b Dose-Ranging Study of Bremelanotide.The journal of sexual medicine · 2019PMID 31277966Accessed 2 Oct 2026
- 7Usefulness of ambulatory blood pressure monitoring to assess the melanocortin receptor agonist bremelanotide.Journal of hypertension · 2017PMID 27977473Accessed 2 Oct 2026
- 8Phase I Randomized Placebo-controlled, Double-blind Study of the Safety and Tolerability of Bremelanotide Coadministered With Ethanol in Healthy Male and Female Participants.Clinical therapeutics · 2017PMID 28189361Accessed 2 Oct 2026
- 9Bremelanotide for female sexual dysfunctions in premenopausal women: a randomized, placebo-controlled dose-finding trial.Women's health (London, England) · 2016PMID 27181790Accessed 2 Oct 2026
- 10Salvage of sildenafil failures with bremelanotide: a randomized, double-blind, placebo controlled study.The Journal of urology · 2008PMID 18206919Accessed 2 Oct 2026
- 11An effect on the subjective sexual response in premenopausal women with sexual arousal disorder by bremelanotide (PT-141), a melanocortin receptor agonist.The journal of sexual medicine · 2006PMID 16839319Accessed 2 Oct 2026
- 12Evaluation of the safety, pharmacokinetics and pharmacodynamic effects of subcutaneously administered PT-141, a melanocortin receptor agonist, in healthy male subjects and in patients with an inadequate response to Viagra.International journal of impotence research · 2004PMID 14999221Accessed 2 Oct 2026
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