PT-141 Half-Life: How Long It Stays in Your System
How long PT-141 stays in the body, how that shapes dosing frequency, and what is known about drug testing.
- Half-life
- approximately 2.7 hours (range 1.9-4.0 h)
- subcutaneous, in people · FDA label (Vyleesi)
- Dosing interval
- Varies by study
- as used in studies
- WADA
- Not listed
- 2026 Prohibited List
- Detection window
- Not found
- None reported as of 2 Oct 2026
PT-141 half-life
A half-life depends on the route (under the skin, into a vein, by mouth or nasal spray) and the species it was measured in, so we report each value with its route and source.
| Route | Half-life | Measured in | Source |
|---|---|---|---|
| subcutaneous | approximately 2.7 hours (range 1.9-4.0 h) | People | FDA label (Vyleesi) |
| intranasal | mean t1/2 1.85 to 2.09 h | People | International journal of impotence research 2004, PMID 14963471 |
| As labelled | approximately 2.7 hours (range 1.9-4.0 h), single subcutaneous dose | People | FDA label (Vyleesi) |
What half-life means
Half-life is the time it takes for the amount of a drug in the blood to fall by half. After one half-life, about 50% is left; after two, about 25%; after four to five, only a few percent remain.
- A long half-life lets a drug be dosed less often, for example once a week.
- A short half-life means levels rise and fall quickly, which is why some peptides are given daily or more often.
- Effects can outlast blood levels, so half-life alone does not tell you how long a drug works.
What it means for dosing frequency
Dosing intervals used in published studies of PT-141:
- as needed before sexual activity, subcutaneous (Human RCT; Journal of women's health 2022, PMID 35230162)
- as needed, subcutaneous (Human RCT; Obstetrics and gynecology 2019, PMID 31599840)
- single doses on days 1, 4 and 7, with or without ethanol, intranasal (Human RCT; Clinical therapeutics 2017, PMID 28189361)
- as desired, subcutaneous (Human RCT; Women's health 2016, PMID 27181790)
Changing the interval changes how much drug builds up between doses, so it is not a free choice.
Drug tests and sport
Not on the WADA Prohibited ListPT-141 (bremelanotide) is not named on the list and is FDA-approved (Vyleesi), so S0 does not apply. It does not fit the named S2 subclasses.
Anti-doping labs use tests built for specific substances. Whether a given test detects PT-141, and for how long, is not reported in the anti-doping literature we checked (as of 2 Oct 2026).
Common questions
How long does PT-141 stay in your system?
Its reported half-life is approximately 2.7 hours (range 1.9-4.0 h) (subcutaneous); mean t1/2 1.85 to 2.09 h (intranasal). Most of a dose is gone after about four to five half-lives.
What is the half-life of PT-141?
Approximately 2.7 hours (range 1.9-4.0 h) (subcutaneous); mean t1/2 1.85 to 2.09 h (intranasal), from the sources cited below.
Is PT-141 on the WADA prohibited list?
No, it is not listed. PT-141 (bremelanotide) is not named on the list and is FDA-approved (Vyleesi), so S0 does not apply. It does not fit the named S2 subclasses.
More on PT-141
Sources
- 1World Anti-Doping Code International Standard Prohibited List 2026World Anti-Doping Agency · 2026wada-ama.orgAccessed 2 Oct 2026
- 2These 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
- 3Double-blind, placebo-controlled evaluation of the safety, pharmacokinetic properties and pharmacodynamic effects of intranasal PT-141, a melanocortin receptor agonist, in healthy males and patients with mild-to-moderate erectile dysfunction.International journal of impotence research · 2004PMID 14963471Accessed 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
- 6Phase 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
- 7Bremelanotide for female sexual dysfunctions in premenopausal women: a randomized, placebo-controlled dose-finding trial.Women's health (London, England) · 2016PMID 27181790Accessed 2 Oct 2026
Found an error? Report a correction.