Research

Peptide Evidence Index 2026

A standardised comparison of the human evidence, clinical-trial status and regulatory status of every compound in the PeptideIndex database.

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What the Peptide Evidence Index is

The Peptide Evidence Index is a structured synthesis of publicly available evidence for the 20 compounds in the PeptideIndex peptide research database. It is not original clinical research and it reports no new data. Its value is the standardised comparison: the same questions asked of every compound, so peptide evidence grades, human studies, clinical trials and regulatory status can be read side by side rather than assembled from scattered sources.

We built it because peptide clinical evidence is unevenly distributed. A few compounds are approved medicines backed by large randomised trials; most rest on animal or mechanistic work, and some have no meaningful direct human evidence at all. Popularity is a poor proxy for evidence, and marketing rarely makes the distinction.

An evidence grade on this site summarises how strong and how directly applicable the body of published research is for a compound. Human randomised evidence carries more weight than observational human data, which carries more weight than animal or in-vitro findings, because only controlled human research can show that an effect seen in a dish or a rodent translates to people at a realistic dose.

Evidence strength is not safety, and it is not suitability for any individual. A well-studied compound can still be unsafe for a given person, and a poorly studied one is not thereby safe — it is simply unknown. Nothing here is medical advice.

Summary statistics

Compounds indexed
20
Strong evidence grade
5
Moderate evidence grade
4
Emerging evidence grade
5
Limited evidence grade
6
With controlled human trial evidence
9
Approved medicine for at least one indication
6
Primary source links catalogued
27

The index

Category

Evidence grade

Human evidence

Peptide Evidence Index 2026 — evidence grade, human evidence, clinical-trial status, regulatory status and primary sources for 20 compounds
PeptideCategoryEvidence gradeHuman evidenceClinical-trial statusRegulatory statusPrimary sources
BPC-157Evidence reviewRecovery & repairEmergingLimited human studies — a registered phase 1 safety/pharmacokinetics study in healthy volunteers; efficacy evidence is predominantly animalRegistered phase 1 trial; no completed positive efficacy programme identifiedNot approved as a medicine; research-compound status in most jurisdictions
TB-500Evidence reviewRecovery & repairEmergingNo direct human trials of marketed TB-500 identified; randomised human trials exist for thymosin beta-4 formulations, which are a different productHuman trials are of topical thymosin beta-4 (RGN-259), not TB-500Not approved for human use; sold for research purposes only
CJC-1295Evidence reviewGrowth hormoneModerateEarly human evidence on GH and IGF-1 secretion; clinical-outcome data limitedEarly-phase human research; no current approval programme identifiedNot approved as a medicine; prohibited in sport
IpamorelinEvidence reviewGrowth hormoneModerateEarly human evidence on GH secretion; no established clinical-outcome evidenceEarly-phase human research; no approved indicationNot approved as a medicine; prohibited in sport
TesamorelinEvidence reviewGrowth hormoneStrongMultiple controlled human trials supporting a specific approved indicationApproved medicine with a completed clinical-trial programmeApproved for a specific medical indication; other uses are off-label
SemaglutideEvidence reviewMetabolicStrongMultiple large controlled human trialsApproved medicine with an extensive phase 3 programmeApproved, prescription-only medicine for specific indications
TirzepatideEvidence reviewMetabolicStrongMultiple large controlled human trialsApproved medicine with an extensive phase 3 programmeApproved, prescription-only medicine for specific indications
RetatrutideEvidence reviewMetabolicStrongPeer-reviewed randomised phase 2 trials; phase 3 outcomes so far company-reported with peer-reviewed publication pendingPhase 3 programme ongoing; phase 2 completed and publishedInvestigational; not approved as a medicine
MOTS-cEvidence reviewMetabolicEmergingHuman data largely observational (endogenous levels); interventional evidence is animal, so this is not human efficacy evidenceNo substantial direct clinical-trial programme identifiedResearch compound; not approved as a medicine
AOD-9604MetabolicLimitedLimited human evidence; no established clinical outcomesEarly-phase human research reported; no approved indicationNot approved as a medicine; permitted as a food additive in some jurisdictions
5-Amino-1MQMetabolicLimitedNo meaningful direct human evidence identifiedNo substantial direct clinical-trial programme identifiedNot an approved medicine or dietary supplement
EpitalonEvidence reviewLongevityLimitedRussian clinical reports have not been independently confirmed; no confirmatory controlled trials identifiedNo independently confirmed clinical-trial programme identifiedNot approved outside Russia/CIS research contexts
SS-31Evidence reviewLongevityModerateRandomised phase 3 trial in primary mitochondrial myopathy (primary endpoints not met) — a disease population, not an ageing or lifespan outcomePhase 3 completed; primary endpoints not metInvestigational; not approved for general use
NAD+Evidence reviewLongevityEmergingRandomised human trials of NAD+ precursors with biomarker endpoints; no lifespan or clinical-outcome evidenceHuman trials with biomarker endpoints; no approval programme for ageingNot an approved medicine for ageing; compounded and sold in clinics
SemaxEvidence reviewCognitiveLimitedHuman use is based largely on Russian clinical literature with limited international replicationNo internationally replicated clinical-trial programme identifiedApproved medicine in Russia; unapproved elsewhere
SelankEvidence reviewCognitiveLimitedHuman use is based largely on Russian clinical literature with limited international replicationNo internationally replicated clinical-trial programme identifiedRegistered in Russia; research-only status elsewhere
GHK-CuEvidence reviewSkin & hairModerateLimited human evidence for topical/cosmetic use; no trials of injectable use identifiedNo substantial clinical-trial programme identified for injectable useWidely used as a cosmetic ingredient; injectable use is unapproved
Melanotan IISkin & hairLimitedEarly human evidence only, alongside documented safety concernsNo approved clinical-development programme identifiedNot approved anywhere; illegal to sell for human use in the UK, EU and US
PT-141Sexual healthStrongMultiple controlled human trials supporting a specific approved indicationApproved medicine with a completed clinical-trial programmeApproved (Vyleesi) for premenopausal HSDD; other uses are off-label
Kisspeptin-10Sexual healthEmergingRandomized controlled human study in healthy men showing endocrine activity; therapeutic efficacy for a clinical indication remains unestablishedControlled human studies published; therapeutic clinical efficacy remains investigationalResearch compound; not approved for human use

How the Peptide Evidence Index works

The index applies the evidence hierarchy PeptideIndex already uses across the site, strongest first:

  1. Human randomised or controlled evidence
  2. Observational human evidence
  3. Animal research
  4. In-vitro and mechanistic evidence
  5. Anecdote and self-report

No new scoring system was created for this page. Grades are read directly from the existing compound profiles, and trial and regulatory descriptors state only what can be verified from catalogued sources. Where no verified primary source is yet catalogued, the row says so rather than implying completeness. Read the full editorial methodology. The index is a structured synthesis of the available evidence, not medical advice.

What the evidence grades mean

Strong
Consistent controlled human evidence, usually with an approved medicine behind it.
Moderate
Some human evidence, but limited in size, scope or outcome quality.
Emerging
Early or indirect human evidence; the bulk of the research is preclinical.
Limited
Little or no reliable human evidence identified for the compound itself.

Full definitions live in the editorial methodology.

Questions this dataset answers

Which peptides have the strongest human evidence?

5 compounds carry the site's highest existing grade: Tesamorelin, Semaglutide, Tirzepatide, Retatrutide, PT-141. That reflects controlled human trial programmes rather than any ranking created for this page. Retatrutide is included on published phase 2 evidence; its phase 3 outcomes are so far company-reported with peer-reviewed publication pending.

Which peptides have limited human evidence?

11 of 20 compounds rely predominantly on early-phase, indirect or preclinical research. TB-500 is a clear example: the randomised human trials in this area studied topical thymosin beta-4 formulations, not marketed TB-500, so they are not direct evidence for it.

Does an evidence grade mean a peptide is safe?

No. Evidence strength and safety are related but separate questions. A grade describes how well an effect has been studied, not whether a compound is safe for a particular person, dose, duration or combination.

Does regulatory approval mean every use is proven?

No. Approval applies to specific products, specific indications and specific jurisdictions. An approved peptide medicine used for an unapproved purpose is not covered by the evidence that secured that approval.

Do longevity peptides have human lifespan evidence?

Not in this dataset. Where human trials exist for longevity-associated compounds, they measure biomarkers, mitochondrial or metabolic outcomes, or disease endpoints. Those are not demonstrations of extended human lifespan.

Citing the Peptide Evidence Index

This page may be cited freely. Publisher: PeptideIndex. Year: 2026.

PeptideIndex. Peptide Evidence Index 2026. A structured comparison of the human, clinical and regulatory evidence across 20 peptide compounds. https://peptide-index.org/research/peptide-evidence-index

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