RECONNECT phase 3 RCT data
A 2019 Obstetrics and Gynecology paper reported two randomised phase 3 trials in 1,202 women, the registrational basis for approval in this indication. Reported in the cited paper.
SourceResearch Use Only. Products listed are not for human or animal consumption. Statements have not been evaluated by the FDA.View full disclaimers →
PT-141, known as bremelanotide, is a melanocortin receptor agonist approved as Vyleesi for acquired hypoactive sexual desire disorder in premenopausal women. It acts centrally on arousal pathways rather than on the vascular system like PDE5 inhibitors.
Vendor listings
Show prices as
56 listings · PT-141
In stock10mgseen 6d ago
In stock3mgseen 6d ago
In stock10mgseen 4d ago
In stock10mgseen 6d ago
In stock10mgseen 4d ago
In stock10mgseen 4d ago
In stock10mgseen 4d ago
In stock10mgseen 6d ago
In stock10mgseen 7d ago
In stock10mgseen 3d ago
In stock10mgseen 4d ago
In stock10mgseen 7d ago
In stock10mgseen 7d ago
In stock10mgseen 4d ago
In stock10mgseen 5d ago
In stock10mgseen 6d ago
In stock10mgseen 5d ago
In stock10mgseen 5d ago
In stock10mgseen 4d ago
In stock10mgseen 4d ago
Overview
PT-141, known as bremelanotide, is a melanocortin receptor agonist approved as Vyleesi for acquired hypoactive sexual desire disorder in premenopausal women. It acts centrally on arousal pathways rather than on the vascular system like PDE5 inhibitors.
What the research reports
Outcomes described across the published PT-141 literature and ongoing study. Read each as research context rather than a promised personal result.
Central arousal mechanism
Activates melanocortin receptors in the brain to influence sexual arousal, working through a different route to PDE5 inhibitors. Reported in research settings.
Approved HSDD use in women
Registrational trials supported approval for acquired, generalised hypoactive sexual desire disorder in premenopausal women. Reported in research settings.
Desire and distress outcomes
Phase 3 subgroup analyses reported improved sexual desire and reduced associated distress across the studied populations. Reported in research settings.
Sustained effect study data
A 52 week open label extension in 684 participants reported sustained improvement with no new safety signals emerging. Described in the research record.
Male erectile study research
A 2008 randomised trial found intranasal bremelanotide improved erectile function in 33.5 percent of sildenafil resistant men against 8.5 percent on placebo.
Dosage and protocol
Protocols use 1 to 2 mg as needed, 45 minutes to 2 hours before activity, with a maximum of one dose in any 24 hour period. Figures describe study protocols, not a personal regimen.
Clinical evidence
The published PT-141 record, labeled by strength so you can see what is settled and what is still emerging.
A 2019 Obstetrics and Gynecology paper reported two randomised phase 3 trials in 1,202 women, the registrational basis for approval in this indication. Reported in the cited paper.
SourceA 2019 open label extension in 684 participants over 52 weeks reported sustained improvement with no new safety signals identified by the investigators. Reported in the cited paper.
SourceA review across the clinical development programme of about 3,500 participants reported mostly mild to moderate events, with nausea leading discontinuation. Reported in the cited paper.
SourceInteractions
Questions
The directory
83 listed
Newsletter · Quarterly
Get notified about new lab results, price drops and supplier coupons before everyone else.
We respect your privacy. No spam.