Sexual Health / research dosage / Last reviewed 2026-06-02

PT-141 Research Dosage: Published Protocol Reference

PT-141 dosage references vary by route and study context. The database lists Subcutaneous injection (FDA-approved): 1.75 mg, As needed, at least 45 min before activity and Subcutaneous (research): 0.5-2 mg, As needed. These are research-context references, not a universal protocol.

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Direct Answer

PT-141 (bremelanotide) is FDA-approved for hypoactive sexual desire disorder in premenopausal women (Vyleesi), providing a regulatory anchor for sexual health research. Phase 3 data in women is solid; male sexual dysfunction data is earlier-stage. For melanocortin-pathway sexual health research, this is the best-evidenced starting point.

Evidence grade
Level A
Research status
FDA Approved
Category
Sexual Health
Best for
Hypoactive sexual desire disorder (women), sexual dysfunction research, melanocortin pathway

Research Dosage References

Half-Life

~2.7 hours.

Evidence Limits

Dosage entries are compiled from labels, published studies, and research-context references where available. For PT-141, the evidence grade is Level A, and the current research status is FDA Approved.

Safety Signals

Evidence Snapshot

Evidence gradeLevel A
Research statusFDA Approved
Best supported outcomesFemale Sexual Desire (Level A), Nausea (Level A), and Male Erectile Function (Level B)
Primary citation count2
Last reviewed2026-06-02

Related Guides

How to Cite This Page

ExaminePeptides. "PT-141 Research Dosage: Published Protocol Reference." Last reviewed 2026-06-02. https://examinepeptides.com/answers/pt-141-research-dosage/

This static answer page is built for fast indexing and direct citation. It summarizes the matching full evidence review and links back to primary sources where the source database includes them.