VIAL
Compound comparison

CJC-1295 vs PT-141

CJC-1295 and PT-141 are both peptide compounds evaluated on Vial: CJC-1295 is available as a compounded preparation with clinical-trial evidence, and PT-141 is FDA approved with FDA-approval-level clinical evidence, offered by 16 and 9 verified providers respectively.

Vial summary · compiled from public records

At a glance

CJC-1295

Category
Peptide
FDA / legal status
Compoundable
Route
Subcutaneous
16providers on Vial →

PT-141

Sold as Vyleesi

Category
Peptide
FDA / legal status
FDA Approved
Route
Subcutaneous
9providers on Vial →

Side by side

FieldCJC-1295PT-141
CategoryPeptidePeptide
Brand namesVyleesi
FDA / legal statusCompoundableFDA Approved
Evidence tierClinical TrialsFDA Approved
Administration routeSubcutaneousSubcutaneous
Compounding accessAvailable through 503A and 503B compounding pharmaciesFDA-approved product, dispensed by prescription
Providers on Vial16 listed9 listed
Typical price band$$ to $$$$$

Verified providers offering each

Ranked by Confidence Rating, Vial’s 0 to 100 score built from federal and state public records. The score evaluates the provider, not the compound.

85+ High Confidence70 to 84 Well Documented50 to 69 Limited ConfidenceUnder 50 Flagged

About each compound

About CJC-1295

A synthetic analog of growth hormone-releasing hormone (GHRH), this 30-amino acid peptide is modified with a drug affinity complex (DAC) that extends its half-life by binding to serum albumin. It stimulates pulsatile growth hormone secretion from the anterior pituitary by activating GHRH receptors. The compound has been investigated in clinical research for growth hormone deficiency and conditions associated with impaired GH/IGF-1 axis function.

About PT-141

A synthetic cyclic heptapeptide melanocortin receptor agonist, bremelanotide (PT-141) acts primarily on MC4 receptors in the central nervous system to modulate sexual arousal pathways. The compound increases sexual desire through direct neurological mechanisms rather than peripheral vascular effects. Its primary clinical application is the treatment of hypoactive sexual desire disorder in premenopausal women.

Descriptions compiled from public FDA records and manufacturer labeling where available. Not medical advice.

This page evaluates compliance signals, not clinical outcomes. Consult a licensed physician before starting any therapy, medication, or treatment. Vial does not provide medical advice.

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