Women's Libido stack
PT-141 + Oxytocin — central desire & connection
1.485.000 ₫
Vial-by-vial breakdown
A female-focused research pairing built around the stronger clinical evidence for PT-141 and the more preliminary social-bonding rationale for oxytocin. PT-141 (bremelanotide) has the clearest women-specific evidence in this stack. Two randomized Phase 3 trials involving 1,267 premenopausal women with acquired, generalized HSDD found statistically significant improvements in sexual desire and reductions in associated distress compared with placebo. The FDA approval of the branded medicine Vyleesi is limited to this defined female population and does not apply to VCP research products. Oxytocin is involved in bonding and social-affiliative signalling, but that biology should not be confused with demonstrated treatment efficacy. Small randomized studies of oxytocin for female sexual function have produced mixed or null results, so any added intimacy or connection benefit remains uncertain. No human trial has tested PT-141 and oxytocin together. The combination is a research rationale rather than a clinically proven stack. Available Small (1 vial of each) or Large (2 vials of each), as vials, pen cartridges (+30%) or a nasal spray (+30%; 5mL Small, 10mL Large).
Dosage
PT-141: 250–500mcg SubQ on-demand · Oxytocin: ~24 IU (≈48 µg) intranasal as needed
Key Features
- Women-specific Phase 3 PT-141 evidence
- Oxytocin connection rationale remains preliminary
- Small (1 vial each) or Large (2 vials each)
- 10% stack discount
Includes key details, half-life data, usage notes and research sources.
Usage Instructions
Subcutaneous injection as recommended. Consult a healthcare professional for protocols tailored to your goals.
Research Highlights
- Backed by scientific research
- Manufactured to pharmaceutical standards
- Used in clinical research settings
- Established safety profile
Safety Information
- •Consult your healthcare provider before use
- •Not intended for pregnant or nursing women
- •Store properly according to instructions
- •Report any adverse effects to your healthcare provider
Source: Kingsberg et al., Obstetrics & Gynecology (2019) — RECONNECT
Clinical Research
Across two randomized Phase 3 trials involving 1,267 premenopausal women with acquired, generalized HSDD, PT-141 produced statistically significant improvements in sexual desire and reductions in distress versus placebo. The evidence applies to PT-141 alone, not the PT-141 + oxytocin combination.
Read full studyAdditional Research
Source: Mesbahi et al., BMC Women's Health (2022) — randomized trial
Oxytocin evidence for female sexual function is limited and mixed. A small randomized trial in breastfeeding women found no statistically significant advantage over placebo for overall sexual function. Route and population differed from this stack, so the result is included as a caution rather than direct evidence.
Read full studyHuman Clinical Trials
- RECONNECT (two phase 3 trials)Obstetrics & Gynecology · 2019
Two identical placebo-controlled trials in women with low sexual desire: significant improvement in desire and reduced distress.
Read the trial1267participants