Evidence Reference

Peptide Evidence-Grade Index

18commonly discussed peptides, graded A–D by one thing only: how much rigorous human clinical evidence exists, not how heavily they are marketed. A high grade means “well-studied,” never “proven to work for you.”

Built and medically reviewed by Charles Kamen, MD, board-certified neurologist ·

Of 18 commonly discussed peptides, only 5 are FDA-approved with multiple Phase 3 trials (semaglutide, tirzepatide, liraglutide, tesamorelin, and bremelanotide), while several of the most heavily marketed, including BPC-157, epithalon, and MOTS-c, have zero completed human efficacy trials. This index grades only the strength and quantity of human clinical evidence for each peptide. It is an evidence-cartography tool, not a treatment guide: a high tier means a molecule has been studied in well-designed human trials, not that it is effective for what it is marketed for. “Studied for” describes the research question a trial asked, never an outcome.

Why grade evidence at all? In clinical medicine, the question “is there good human data?” always comes before “does it work?”, and the answer lives on a spectrum. A large Phase 3 randomized controlled trial in thousands of people counts for far more than a single small pilot, which counts for far more than an animal study, which counts for far more than anecdote or a registry entry for a trial that has not finished. Peptide marketing routinely collapses that spectrum: a rat result is repeated until it sounds like a clinical fact, and a recruiting trial is described as if it were completed evidence. Grading each peptide by the highest level of completed human evidence it actually has is how a physician keeps that honest.

How this site grades peptides, in one sentence: we ask what is the most rigorous finished human evidence on record for each molecule. FDA approval with multiple Phase 3 trials is Tier A, completed human RCTs without U.S. approval is Tier B, pilot or small-study human data is Tier C, and animal or laboratory evidence only is Tier D. Trial counts are approximate and point-in-time; the tier is firm. A peptide never moves up a tier because of marketing, patient testimonials, or a registered-but-unfinished study. If you want the deeper safety and FDA-status context for any of these, see our physician-reviewed guides on which peptides are FDA-approved, whether peptide therapy is safe, and the FDA peptide compounding status tracker.

Why evidence grading matters

Human trials outrank animal data — a rat result is a hypothesis, not a clinical fact.

A registered trial is not finished evidence; recruitment does not equal results.

FDA approval with multiple Phase 3 RCTs is the gold standard, not a marketing claim.

Marketing intensity often runs inverse to evidence — the loudest peptides are frequently Tier C or D.

Grading evidence is separate from judging efficacy — well-studied is not the same as right for you.

Honest protocols are built on confidence levels: high-tier evidence carries real numbers; low-tier is a hypothesis.

The grading rubric

Each peptide is graded by the highest level of completed human evidence that exists for it, regardless of how popular or heavily marketed it is.

A
FDA-Approved, Multi-RCT

FDA-approved for at least one indication, supported by multiple completed Phase 3 randomized controlled trials. The gold standard of human evidence.

B
Human RCT Evidence (not U.S.-approved)

Not FDA-approved for the use in question, but has one or more completed human RCTs in the peer-reviewed literature — or is approved abroad / for a narrow historic indication on RCT data.

C
Human Pilot / Small-Study

Human data exists but is limited to pilot trials, small or early-phase studies, observational cohorts, or non-blinded programs. Clinical outcomes are not robustly established.

D
Preclinical Only

Evidence is animal or laboratory only. No completed registered human trial demonstrating clinical outcomes — even if early-phase human trials are now registered or recruiting.

Tie-breaker: a peptide is graded by its strongest completed human evidence for a defined clinical question. A registered-but-not-completed trial does not lift a peptide out of Tier D; recruitment is not evidence.

The index

Peptide human-evidence grade index — LiveNow Longevity, compiled July 24, 2026. Trial counts are approximate, point-in-time.
PeptideTier~Completed human trialsStudied for (neutral)Evidence note
Semaglutide (Ozempic / Wegovy)ADozens of Phase 3 RCTs (STEP, SUSTAIN, PIONEER)Type 2 diabetes; chronic weight management; cardiovascular riskAmong the most extensively trialed peptides in medicine; FDA-approved 2017 (diabetes), 2021 (weight).
Tirzepatide (Mounjaro / Zepbound)ADozens of Phase 3 RCTs (SURPASS, SURMOUNT)Type 2 diabetes; chronic weight management; obstructive sleep apneaDual GIP/GLP-1 agonist; FDA-approved 2022 (diabetes), 2023 (weight), 2024 (OSA).
Liraglutide (Victoza / Saxenda)AMultiple Phase 3 RCTs (SCALE; LEADER outcomes)Type 2 diabetes; chronic weight management; cardiovascular riskFirst daily GLP-1; FDA-approved 2010 (diabetes), 2014 (weight); now has generics.
Tesamorelin (Egrifta)A2 pivotal Phase 3 RCTsReduction of excess visceral abdominal fat in HIV-associated lipodystrophyGHRH analog; FDA-approved 2010 — the only FDA-approved growth-hormone-releasing peptide. Narrow indication, but multi-RCT.
Bremelanotide / PT-141 (Vyleesi)A2 pivotal Phase 3 RCTs (RECONNECT 1 & 2)Acquired, generalized HSDD in premenopausal womenMelanocortin-4 agonist; FDA-approved 2019. The consumer "PT-141" sold for general libido use is off-label / non-FDA-approved.
Thymosin alpha-1 (Zadaxin)B30+ human trials incl. multiple RCTsHepatitis B & C (adjunct); immune modulation; sepsis (investigational)Approved in 35+ countries but never FDA-approved in the U.S. Unusually large RCT base for a non-U.S.-approved peptide.
RetatrutideBMultiple Phase 3 RCTs completed/reporting (TRIUMPH)Chronic weight management; type 2 diabetes; cardiometabolic riskTriple GLP-1/GIP/glucagon agonist. Strong Phase 3 data, but investigational — not yet FDA-approved as of June 2026 (NDA anticipated later in 2026).
TB-500 / Thymosin beta-4CA few small trials — for the topical drug RGN-259, not consumer "TB-500"Wound/tissue repair; dry eye; neurotrophic keratopathyCritical distinction: human trials used RGN-259, a topical ophthalmic Tβ4 drug — not the injectable "TB-500" sold to consumers, which has no completed human efficacy trials. The well-known cardiac-repair signal is animal data (Bock-Marquette, Nature 2004). A 2024 Phase 3 dry-eye program missed its primary endpoint.
CJC-1295C~1 early-phase human PK/PD RCTShort-term growth-hormone / IGF-1 secretion (pharmacodynamics)Human data confirms it raises GH/IGF-1 short-term; no completed clinical-outcome trials. The one outcome trial registered was terminated.
IpamorelinC~1–2 small early-phase human studiesGrowth-hormone secretion (pharmacodynamics)Early human data shows GH secretion; no completed outcome trials. There are zero rigorous human trials of the popular CJC-1295 + ipamorelin combination.
Sermorelin (formerly Geref)CSmall therapeutic & GHRH studiesHistoric: pediatric growth-hormone-deficiency diagnosis & treatmentWas FDA-approved, discontinued 2008 for business — not safety — reasons. Current adult/anti-aging use is off-label via compounding; no large modern RCTs for those uses.
GHK-Cu (copper tripeptide)C~7 human studies, ~1–2 RCTsTopical: skin appearance / photoaging; wound healingA topical human signal exists, but landmark cosmetic trials were industry-sponsored and largely conference-presented; results are mixed. Not in major wound-care guidelines.
SemaxCMultiple Russian clinical trialsIschemic stroke adjunct; cognition; neuroprotection (as studied in Russia)Regulatory-approved in Russia for stroke/encephalopathy. Evidence is concentrated in Russian institutions and largely not independently replicated in Western RCTs; not FDA-approved.
SelankCRussian Phase 3-level trialsAnxiety / generalized anxiety disorder (as studied in Russia)Approved in Russia as an anxiolytic. Minimal English-language peer-reviewed RCT data; not FDA-approved.
MOTS-cD0 completed outcome trials; Phase 1/2 registered & ongoingInsulin sensitivity; metabolic health; exercise-related metabolismStrong animal and human-observational data, but no completed human efficacy trial. A Phase 2a in prediabetes is underway, not finished. Registration is not completed evidence.
BPC-157D0 completed registered human efficacy trialsTissue/tendon/muscle healing; gut protection (preclinical questions)Despite very heavy marketing, BPC-157’s evidence is almost entirely animal/in-vitro. The often-cited ligament-healing paper is a rat study (Cerovecki, J Orthop Res 2010). The 2015 Phase 1 was cancelled without results; a 2025 hamstring trial is registered but not completed. Not FDA-approved.
Epithalon / EpitalonD0 trials registered on ClinicalTrials.govAging biomarkers; telomere biology; pineal/longevity researchAn in-vitro telomerase signal exists in human cell cultures. Human "longevity" claims trace to non-blinded, non-randomized Russian observational programs, often using the extract Epithalamin rather than synthetic Epitalon.
NAD+ / NMN (non-peptide contrast)C~8–9 completed human RCTs (small, early-phase)NAD+ metabolism; insulin sensitivity; muscle function; healthy agingIncluded as a non-peptide contrast. Human trials confirm NMN raises blood NAD+ levels and is well tolerated; clinical-outcome evidence is preliminary. A dietary supplement, not an FDA-approved drug.

How this index is built: compiled and reviewed by Charles Kamen, MD from ClinicalTrials.gov, PubMed / PubMed Central, and U.S. FDA records. Trial counts are approximate and reflect a point-in-time read of public registries (June 2026); the tiers are firm, the exact counts carry the uncertainty. The row for systemic “TB-500” is consolidated into the thymosin beta-4 entry, since they are the same/overlapping molecule — this keeps the index honest rather than padding the count.

Scope & compliance: this index grades how much human evidence exists, never whether a peptide “works,” is safe for you, or is right for any condition. It contains no doses, no titration schedules, no patient outcomes, and no protocols. Many peptides here are not FDA-approved. This is educational information about the state of clinical research — not medical advice. Decisions about any peptide should be made with a licensed physician who can evaluate your individual situation.

How we use evidence grades in your protocol

An evidence grade is not a prescription — but it shapes how a thoughtful physician builds your plan. A Tier A medication is one where dosing, expected benefits, and risks have been measured in thousands of people, so Dr. Kamen can plan around real numbers and monitor you against known benchmarks. A Tier B peptide may be appropriate when its human RCT data aligns with your situation and an FDA-approved alternative does not fit. Tier C is a calculated, monitored adjunct at most; Tier D is, in most cases, worth skipping until the human evidence catches up to the marketing.

Practically, that means the grade informs three things: whether something is offered at all, how it is monitored if it is, and what you are told to expect. We do not sell a checkout cart of “stacks.” If a heavily marketed peptide is Tier D, you will hear that directly — along with what an evidence-based alternative looks like for your goals. Care starts with an $88 evaluation and is built around your labs, history, and the actual state of the science — not what is trending on social media. For the full service overview, see physician-supervised peptide therapy.

Peptide evidence in Las Vegas

The evidence on this page does not change by ZIP code — but the marketing pressure absolutely does. Las Vegas has one of the densest concentrations of med-spa, concierge, and direct-to-consumer peptide offerings in the country, and the most aggressively advertised molecules (BPC-157, MOTS-c, epithalon) are very often the ones with the weakest human evidence. That is the gap this index exists to close: a single, physician-maintained map of what has actually been studied in people, so a Las Vegas patient can tell the difference between a proven medication and a hypothesis with a price tag.

Whether you visit our southeast Las Vegas clinic at Eastern Avenue and the 215 from Henderson, Summerlin, Green Valley, or anywhere in the valley — or meet Dr. Kamen by secure telehealth across Nevada — the grading conversation is identical: what the research shows, what tier it sits in, and what that means for your specific goals. No hype, no “research use only” injectables, no stacks sold by the bundle. Just an honest, board-certified read on the evidence. Visit our Las Vegas peptide clinic to start.

Peptide Evidence FAQ

What is peptide evidence grading?

Evidence grading is a way of ranking how much rigorous human clinical research exists for a given peptide — from FDA approval with multiple Phase 3 trials (Tier A) down to animal and laboratory data only (Tier D). It is borrowed from the same hierarchy clinical medicine uses everywhere: randomized controlled trials in humans count for more than animal studies, and a registered-but-unfinished trial is not the same as completed evidence. Crucially, an evidence grade measures how well-studied a molecule is — never whether it works for you. A Tier A peptide is well-tested; whether it is appropriate for you is a separate medical decision.

Does BPC-157 have human clinical trials?

No — as of July 2026, BPC-157 has no completed registered human efficacy trials on ClinicalTrials.gov. A 2015 Phase 1 safety trial was cancelled without published results, and a 2025 hamstring-strain trial is registered but not yet completed. Essentially all BPC-157 evidence to date is from animal and laboratory studies — the frequently cited ligament-healing result is a rat model (Cerovecki, J Orthop Res 2010) — which is why BPC-157 is graded Tier D (preclinical only) in this index.

Which peptides have the strongest human evidence?

The GLP-1-class incretin peptides — semaglutide, tirzepatide, and liraglutide — have the strongest human evidence, each backed by dozens of completed Phase 3 randomized controlled trials and FDA approval (all Tier A). Semaglutide’s STEP program alone produced multiple landmark trials (e.g., Wilding et al., NEJM 2021). Tesamorelin and bremelanotide are also Tier A but for narrow, specific FDA-approved indications.

Are BPC-157, TB-500, and semaglutide well-studied?

Not equally, and that is the whole point of grading them. Semaglutide is among the most extensively trialed peptides in medicine (Tier A, FDA-approved, dozens of Phase 3 RCTs). TB-500 / thymosin beta-4 is Tier C: its human data comes almost entirely from a topical eye drug (RGN-259), not the injectable sold to consumers, and its famous cardiac-repair signal is animal data (Bock-Marquette, Nature 2004). BPC-157 is Tier D — preclinical only, with zero completed human efficacy trials despite heavy marketing. Same word "peptide," very different evidence.

Why do some clinics oversell peptides?

Because peptides that are not FDA-approved can be compounded and sold with wide margins, and marketing language easily blurs the line between an animal study and a proven human treatment. A rat ligament result gets repeated until it sounds like a clinical fact; a registered-but-incomplete trial is described as if it were finished evidence. Evidence grading is the antidote: it separates how heavily something is marketed from how well it has actually been studied in people. If a clinic cannot tell you the tier of evidence behind what it is selling, that is a signal.

How do evidence grades affect my protocol?

They set honest expectations about confidence. A Tier A medication is one where dosing, benefits, and risks have been measured in thousands of people, so a physician can plan around real numbers. A Tier C or D peptide is a hypothesis — it may be reasonable as an adjunct, or it may be worth skipping entirely, but it should never be sold as if the outcome were settled. At our practice, the grade informs whether something is offered at all, how it is monitored, and what we tell you to expect — not what shows up on an invoice.

Are peptides like sermorelin, CJC-1295, and ipamorelin FDA-approved?

No — sermorelin was historically FDA-approved for a pediatric use but was discontinued in 2008 for business reasons and is now used off-label via compounding. CJC-1295 and ipamorelin have never been FDA-approved; their human data is limited to small early-phase studies showing growth-hormone elevation, with no rigorous human trials of the popular combination. All three are graded Tier C.

Does "studied for" mean a peptide is effective for that?

No — "studied for" means a clinical trial asked a research question about that topic, not that the peptide works, is safe for you, or is approved for that use. This index grades how much human evidence exists, never whether a peptide is effective. Always consult a licensed physician.

Is thymosin alpha-1 FDA-approved?

No — thymosin alpha-1 (Zadaxin) is approved in more than 35 countries and has an unusually large clinical-trial base, but it has never received FDA marketing approval in the United States. It is graded Tier B.

Is peptide evidence grading relevant in Las Vegas, Henderson, or Summerlin?

Yes — the evidence does not change by ZIP code, but the marketing pressure does. Las Vegas has one of the densest concentrations of med-spa and concierge peptide offerings in the country, and the most heavily advertised products (BPC-157, MOTS-c, epithalon) are often the ones with the least human evidence. Whether you come to our southeast Las Vegas clinic at Eastern Ave and the 215 from Henderson, Summerlin, Green Valley, or anywhere in Nevada — or meet Dr. Kamen by secure telehealth — the grading conversation is the same: what the research actually shows, and what that means for your specific goals.

Related reading: Which peptides are FDA-approved? · Longevity drug evidence grades · The 12 hallmarks of aging · Senolytics evidence grades · Biological age tests compared · FDA peptide compounding status tracker · Is peptide therapy safe? · Peptide regulatory status tracker

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