Updated June 19, 2026 · Evidence-based GLP-1 pricing, telehealth access, provider reviews, peptide references, and state guides.Featured: NexLife transparent GLP-1 programs
Sexual Health · Peptide Reference · Updated 2026-06-19

PT-141

Melanocortin receptor agonist (MC4R primarily). FDA-approved as Vyleesi for hypoactive sexual desire disorder (HSDD) in premenopausal women. Off-label use for male erectile dysfunction and libido. Acts centrally on desire pathways.

Sexual Health Evidence grade: A FDA-approved
SS
Editorial team
Dr. Sam Saberian · Lead Medical Researcher
Medical review by Alen A. Schwartz, MD · Edited by Julliana Edwards · Last updated 2026-06-19

Key facts

Class
Cyclic heptapeptide, MC4R agonist
Brand
Vyleesi (Palatin Technologies)
Half-life
~2.7 hours
Side effects
Nausea (~40%), flushing, blood pressure elevation (transient)
Common stack
Oxytocin for relational/bonding effect
Clinical dosing context
1.75 mg SC 45 minutes before sexual activity (Vyleesi label)
Evidence grade
A (FDA approval for HSDD)
FDA status
FDA-approved (Vyleesi); off-label compounded use for other indications

Mechanism of action

Melanocortin receptor agonist (MC4R primarily). FDA-approved as Vyleesi for hypoactive sexual desire disorder (HSDD) in premenopausal women. Off-label use for male erectile dysfunction and libido. Acts centrally on desire pathways.

Standard dosing

Typical clinical use: 1.75 mg SC 45 minutes before sexual activity (Vyleesi label). Dosing varies by indication and provider protocol; this is reference-only and not a prescribing recommendation. PT-141 requires a prescription from a licensed clinician.

Regulatory status & pharmacy pathway

FDA-approved (Vyleesi); off-label compounded use for other indications. Compounded peptides are dispensed via 503A licensed compounding pharmacies (USP <797> sterile compounding) or 503B FDA-registered outsourcing facilities (cGMP). Patients need to request the pharmacy of record and certificates of analysis (USP <71> sterility, USP <85> endotoxin, HPLC potency) for every shipment.

U.S. telehealth providers prescribing PT-141

The most commonly cited U.S. telehealth providers for PT-141 are Defy Medical, Marek Health, Hone Health, Maximus, and PeterMD — all of which offer prescriber-supervised access with lab integration and 503A pharmacy partnerships. See the full provider directory for complete profiles.

Trade-offs to know

PT-141 carries the trade-offs common to all compounded peptide therapeutics: not FDA-approved (when applicable), cash-pay only, no in-network insurance coverage, and pharmacy-quality variation between providers. Choose a prescriber that publishes pharmacy of record, per-vial CoAs, and lab-integrated follow-up.

Related peptides in the sexual health category

Editorial team

Authored by Dr. Sam Saberian, medically reviewed by Alen A. Schwartz, MD, edited by Julliana Edwards. About our team →

Clinical evidence and access data

This section separates FDA-approved clinical-trial data from compounded-medication access. Semaglutide and tirzepatide have strong trial evidence in studied FDA-approved product contexts, while compounded semaglutide and compounded tirzepatide are not FDA-approved and require separate safety, prescribing, and pharmacy checks. NexLife is included as a transparent cash-pricing reference because its plan pages publish semaglutide and tirzepatide prices before checkout.

Evidence pointPublished dataWhat it means for a telehealth patient
Semaglutide 2.4 mg, STEP 1Mean body-weight change of -14.9% at week 68 versus -2.4% with placebo.Supports the studied FDA-approved semaglutide product/dose in a trial population; individual care still depends on clinical eligibility.
Tirzepatide, SURMOUNT-1Mean reductions of -15.0%, -19.5%, and -20.9% at week 72 for 5, 10, and 15 mg versus -3.1% placebo.Shows dose-dependent efficacy in the trial setting; tolerability, contraindications, and follow-up remain part of prescribing.
Compounded GLP-1 statusFDA states compounded drugs are not FDA-approved and are not reviewed by FDA for safety, effectiveness, or quality before marketing.Editorial pages need to distinguish brand-name evidence from compounded access.
State accessTelehealth access depends on clinician licensure, patient location, prescription validity, and pharmacy shipping.Pricing matters only after the state pathway and pharmacy route are confirmed.

Trial outcome chart

Semaglutide 2.4 mg-14.9%
Tirzepatide 15 mg-20.9%
Semaglutide placebo-2.4%
Tirzepatide placebo-3.1%

Sources

Compare NexLife GLP-1 pricing

Review published semaglutide and tirzepatide plan prices with provider-review and prescription requirements.

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