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US Peptide Guide

Editorial standards

How US Peptide Guide evaluates, grades, and cites evidence. Applied uniformly across every peptide page so comparisons are meaningful.

Four-tier evidence framework

Tier 1FDA-Approved
  • Completed Phase 3 clinical trials
  • FDA approval for at least one indication
  • Prescribable under standard protocols

Pages in this tier still document FDA-approved uses separately from off-label uses.

Tier 2Clinically Studied
  • Multiple human RCTs with combined n > 50
  • Available through licensed 503A or 503B compounding
  • Replicated findings in peer-reviewed journals

Single-study findings, however large, may not qualify if unreplicated.

Tier 3Limited Human Evidence
  • At least one published human study (case report, small cohort, or pilot RCT)
  • Strong mechanistic or animal data supporting the claimed effect
  • No serious safety signals from available human exposure

Most currently compoundable peptides fall here. Human data exists but is early.

Tier 4Animal Data Only
  • No published human clinical trials
  • Mechanism inferred from animal models only
  • May have anecdotal human reports but no systematic study

Tier 4 does not mean ineffective — it means unstudied in humans.

Citation policy

Every factual claim on a peptide page must link to a numbered citation. No assertion ships without a reference or an explicit qualifier ("no human data available", "animal data only").

PubMed / MEDLINE

Preferred for all biological claims. PMID required. Title, authors, and year verified before inclusion.

FDA documents

Federal Register notices, CDER letters, Compounding Bulk Drug Substances lists. URL and date required.

ClinicalTrials.gov

Used to document ongoing or completed trials. NCT number required. Not a substitute for published results.

Named expert positions

Public statements by identified clinicians or researchers, with source URL, date, and credential. Paraphrased — not quoted — with a ≤ 15-word position summary.

What reference pages never include

  • Dosing protocols or administration guidance — belongs with a prescriber
  • Vendor or product recommendations
  • Blended evidence summaries that mix animal and human data
  • Marketing claims or testimonials