How we grade evidence: four questions, never one score

In short

About 5 minutes for the short version; 12 with every detail open.

  • Every compound gets four separate grades. We never add them up into one score.
  • Four questions: tested in people? How much lab research? How many research groups? How well are harms known?
  • One score would hide the shape: many rat studies from one lab, and almost no data in people.
  • Badges in the text say what each claim rests on: cells, animals or people.
  • A grade changes when new evidence is published. Every change is logged with its date.
Last reviewed
Three measuring scales side by side on a white surface: the end of a yellow tape measure, a pale blue tape marked in centimetres and a metal ruler, each marked differently.
Three rulers, each with its own scale. We grade evidence on four scales and never add them up. Photo: William Warby from London, England, 3cm (Wikimedia Commons) CC BY 2.0 Image details

Each section starts with the short answer. The rest is folded under “In detail”.

This is the rubric behind the evidence profile on every compound page. It sets out what we grade, the rule and threshold for each grade, what the claim badges in the text mean, and where the rubric stops being useful.

Why four questions and not one score

Why not give each compound a simple score?

Because one number hides where the evidence is strong and where it is missing.

Evidence profile

Four separate questions. Not a score.

Human clinical evidence How far has it been tested in people?
Case reports only (step 2 of 6)
Preclinical volume How much laboratory and animal research exists?
Extensive (step 3 of 3)
Source independence How many independent groups produced it?
One group dominates (step 1 of 3)
Safety characterisation How well do we know the harms in humans?
Uncharacterised (step 1 of 3)
In detail: Why these grades: the reason for each step , about 2 minutes to read
Human clinical evidence
Case reports. The only published human data are four small reports without a comparison group: three led by the same US clinician (16, 12 and 2 people), and one on 3 dental patients who received BPC-157 mixed with four other drugs. A randomised phase 2 trial in 53 people with ulcerative colitis exists only as a 2005 conference abstract, and a placebo-controlled phase 1 study in 32 healthy men only as earlier abstracts. Neither was published in full, so under our rubric they do not count as published phase 1 or phase 2 trials.
Preclinical volume
Extensive. By our count on 20 October 2026, PubMed holds about 160 primary laboratory and animal studies of BPC-157, far above the threshold of 50.
Source independence
Single group dominant. Authors from one group at the University of Zagreb appear on about 140 of roughly 160 primary experimental papers (about 85%). About 20 come from groups outside Zagreb, few of which repeat the group's experiments directly. The only independent test of the rat Achilles-tendon claim (2026) found no statistically significant effect on tendon strength or overall tissue scores, though one collagen measure did differ.
Safety characterisation
Uncharacterised. The published human studies are tiny and short, and most do not say how safety was monitored; the FDA concluded in 2026 that the clinical safety information is insufficient to characterise the safety profile. The animal toxicology comes from one laboratory and lasts 28 days at most.

We never add these up. A compound can have a large animal literature from one laboratory and no human data at all — that is a specific situation, and a single number would hide it. How we grade evidence

BPC-157 shows why. It has a large animal literature, about 160 primary studies. About 85 in 100 of them come from one research group. The only published human data are a few small reports without a comparison group, plus trials known only from short conference abstracts.1,2,3 An average of those facts would read “medium” and describe none of them.

In detail: What a single score would hide , about 1 minute to read

The four grades together have a shape, and the shape is the information. Two compounds with the same “average” can be in completely different situations:

Two very different situations could get the same average score. Four grades keep them apart.
Compound A (the BPC-157 pattern)Compound B (an invented example)
Tested in peopleCase reports onlyA published phase 2 trial
Lab and animal researchExtensive: more than 50 studiesMinimal: fewer than 10
Research groupsOne group dominatesA few groups
Harms in peopleUncharacterisedPartial
What it meansMuch animal work, little of it independently checked, almost nothing in peopleLittle animal work, but a real controlled test in people

A star rating would put both somewhere in the middle. A reader deciding whether to trust an effect, or how cautious to be about harm, needs to know which situation applies. So the four grades sit side by side and are never added, averaged or ranked.

The grades describe the published evidence. They are not a verdict on whether a compound works, and not a judgement of the people who did the research: for BPC-157, see the Croatian lab.

The four questions, and how each grade is given

How is each grade decided?

By a written rule for each question, with thresholds, applied to what has been published.

Human clinical evidence

How far has it been tested in people?

  1. None published No published study in humans.
  2. Case reports only Only individual cases or small uncontrolled series. These can raise questions; they cannot answer them.
  3. Phase I (safety, small) Small studies, usually in healthy volunteers, mainly about safety and how the body handles the compound.
  4. Phase II (dose and early effect) Studies in patients to find doses and look for early signs of effect, usually with a control group.
  5. Phase III (large controlled trials) Large randomised controlled trials designed to test whether it works and how often harm occurs.
  6. Authorised by a regulator A medicines regulator has reviewed the full data and authorised it for specific uses.

Preclinical volume

How much laboratory and animal research exists?

  1. Minimal Fewer than about 10 published primary studies in cells or animals.
  2. Moderate Roughly 10 to 50 published primary studies.
  3. Extensive More than about 50 published primary studies.

Source independence

How many independent groups produced it?

  1. One group dominates Most primary studies come from one research group. Their errors, if any, are repeated rather than caught.
  2. A few groups Two to four groups produced most of the work.
  3. Broadly replicated Many independent groups, and key findings have been reproduced.

Safety characterisation

How well do we know the harms in humans?

  1. Uncharacterised No systematic human safety data. Absence of reported harm is not evidence of safety.
  2. Partial Some human exposure data, short-term or small. Rare and long-term harms are unknown.
  3. Well characterised Large trials plus ongoing post-marketing surveillance. Rare harms are still being learned.

Each grade comes with a short reason on the compound page (“Why these grades”). The rules below are the ones our editors apply. When a compound falls between two steps, we say so in the reason instead of hiding the judgement.

In detail: The full rules, with thresholds , about 3 minutes to read
AxisValuesAssigned by
Human clinical evidencenone · case reports · phase 1 · phase 2 · phase 3 · authorisedThe highest completed and published human evidence. Registered but unpublished trials do not count. “Authorised” means a regulator has granted marketing authorisation somewhere, for some indication.
Preclinical volumeminimal (fewer than 10 published animal or cell studies) · moderate (10 to 50) · extensive (more than 50)A count of primary preclinical publications, not reviews
Source independencesingle group dominant (more than about 70% of primary studies from one group) · few groups (2 to 4 groups account for most) · broadly replicated (many independent groups, and key findings replicated)The authors and affiliations of the primary studies
Safety characterisationuncharacterised (no systematic human safety data) · partial (some human exposure data, short-term or small) · well characterised (large trials plus post-marketing surveillance)Human data only

Human clinical evidence

We take the highest level of human evidence that is both completed and published. A trial that is registered, or reported only as a conference abstract, does not count, because nobody outside can check its methods and results. BPC-157 is the clearest case: a randomised phase 2 trial in 53 people with ulcerative colitis exists only as a 2005 conference abstract, so the grade is “case reports”, not “phase 2”.3 “Authorised” means a medicines regulator has granted marketing authorisation somewhere for some use. It describes the whole programme of trials behind that decision, not every use people put the medicine to.

Preclinical volume

We count primary laboratory and animal publications: studies that report their own experiments. Reviews, commentaries and letters are left out, because a review that repeats a study is not a second experiment. The thresholds are fewer than 10, 10 to 50, and more than 50. For BPC-157 we searched PubMed, removed records tagged as reviews, comments, letters, editorials or errata, sorted the rest by hand, and counted about 160 primary laboratory and animal studies.1

Source independence

We look at who wrote the primary studies. If more than about 70% come from one group (counting its collaborators), the grade is “single group dominant”. If two to four groups account for most of the work, it is “few groups”. “Broadly replicated” needs many independent groups and repeats of the key findings. Independence matters because one group’s shared methods, models and expectations can carry the same error into every study it publishes; a second laboratory with its own methods is less likely to repeat that error. When independent scientists have tried to repeat published preclinical findings, many did not hold up.4,5

Safety characterisation

We use human data only. Animal toxicology tells you what to look for, not what happens in people. “Uncharacterised” means no systematic human safety data. “Partial” means some exposure in people, but short-term or small. “Well characterised” needs large trials plus monitoring after the medicine reaches the market, because only then are enough people exposed for long enough to see uncommon harms.

Every compound side by side

How do the compounds compare?

The table shows all four grades for every compound. Sorting arranges them; it never ranks them.

Sorting arranges compounds by one axis at a time. It does not rank them: the axes are deliberately not combined.

Evidence profiles of all compounds on this site
Compound Human clinical evidencePreclinical volumeSource independenceSafety characterisation
AOD-9604 Phase II (dose and early effect) Minimal One group dominates Partial
BPC-157 Case reports only Extensive One group dominates Uncharacterised
CJC-1295 Phase I (safety, small) Minimal One group dominates Partial
Epitalon Phase II (dose and early effect) Extensive One group dominates Uncharacterised
GHK-Cu Phase II (dose and early effect) Extensive Broadly replicated Uncharacterised
Hexarelin Phase II (dose and early effect) Extensive A few groups Partial
Ipamorelin Phase II (dose and early effect) Moderate A few groups Partial
KPV None published Moderate A few groups Uncharacterised
Melanotan II Phase II (dose and early effect) Extensive Broadly replicated Partial
MOTS-c None published Extensive Broadly replicated Uncharacterised
NAD+ precursors Phase III (large controlled trials) Extensive Broadly replicated Partial
PT-141 Authorised by a regulator Minimal A few groups Partial
Retatrutide Phase III (large controlled trials) Moderate A few groups Partial
Selank Phase II (dose and early effect) Moderate A few groups Uncharacterised
Semaglutide Authorised by a regulator Extensive Broadly replicated Well characterised
Semax Phase II (dose and early effect) Extensive A few groups Uncharacterised
SS-31 Authorised by a regulator Extensive Broadly replicated Partial
TB-500 Case reports only Moderate A few groups Uncharacterised
Tesamorelin Authorised by a regulator Minimal A few groups Partial
Thymosin alpha-1 Authorised by a regulator Extensive Broadly replicated Partial
Tirzepatide Authorised by a regulator Extensive Broadly replicated Well characterised

Read the table one column at a time. A compound can be “authorised” for human evidence and still depend on one company for its key trials; another can have many animal studies and nothing in people. Each compound page explains its own grades.

In detail: Where the rubric needed a judgement call , about 1 minute to read

No rubric fits every case. Two examples from this site:

  • Retatrutide has published phase 3 results, but every human trial was sponsored and largely written by one company, while about 15 independent laboratories have each published one or two small animal or tissue studies.6 “Few groups” is the closest fit for independence, but it is a judgement: the key human findings have not been repeated outside the company. The compound page says so in its reason for the grade.
  • Semaglutide is graded “broadly replicated” although the manufacturer paid for every pivotal trial. The compound page gives the reason: the core effects on blood sugar and weight have been reproduced in studies without company authors, and the main safety questions were tested by independent academic groups and by regulators.7,8,9 Funding and independence are related, but they are not the same question (see conflicts of interest).

In such cases the written reason on the compound page carries more information than the grade itself. See the retatrutide and semaglutide pages.

What the badges in the text mean

What do the small labels next to claims mean?

They say what kind of evidence each claim rests on: an idea, cells, animals or people.
Each claim has a label for what it rests on, from an idea to large trials.
Label in the textWhat it meansWhat it does not mean
HypothesisProposed, not shown in any experimentThat it is false
CellsShown in cells or tissue in the laboratoryThat it happens in a living body
AnimalsShown in animal studiesThat it happens in people
Humans, limitedSeen in people in case reports or small uncontrolled studiesThat the treatment caused it
Human trialsShown in controlled human trialsThat it holds for every group of people, or for every use
EstablishedEstablished in large trials and authorised useThat rare or long-term harms are all known

The steps in each compound’s mechanism chain use a shorter scale: hypothesised, in cells, in animals, in humans. Each step’s label says how well the link into that step has been shown. In the animated explainers, a solid line means shown in people, long dashes shown in animals or cells, and short dashes an idea.

In detail: How the labels are used , about 1 minute to read

A label goes on every claim about what a compound does or how it works. It describes the claim, not the compound: on a single page, one claim can be marked “Animals” and the next “Human trials”. A claim that reports a rat study is labelled “Animals” even when the compound is an authorised medicine, because the label is about that sentence’s evidence.

The mechanism chain on a compound page is read link by link. A chain can be well shown at the first step (the molecule binds its receptor, measured in cells) and only hypothesised at a later one (that this binding is what heals a tendon). The weakest link limits the whole chain: a pathway is only as well established as its least-tested step. That is why each step carries its own label.

What the grades cannot tell you

Does a good grade mean a compound is harmless?

No. A grade describes how much is known. It does not say that harm is absent.
What a grade says, and what it does not.
A grade saysIt does not say
How far testing in people has goneThat the compound works for you
How many lab and animal studies existThat those studies were well done
How many groups did the researchThat any one study is right or wrong
How well harms in people are knownThat a product sold under the name contains what was studied
“Well characterised”That every rare or long-term harm is known

Sources 10, 11, 12, 13

Counting studies is not judging their quality. And the grades are about the molecule as it was studied, not about a vial: a product from outside the legal supply chain can contain a different amount, or a different substance (see product risk).

In detail: Counting is not quality, and known is not complete , about 2 minutes to read

Counting is not quality

“Extensive” preclinical volume means there are more than 50 primary studies, not that they are good. In animal research many studies do not report randomisation, blinding or how their size was chosen, and published animal studies lean towards positive results.10,14 When independent scientists tried to repeat landmark preclinical findings, many did not hold up.4,5 That is why preclinical volume is always read together with independence, and why the translation gap explains what animal studies can and cannot show.

Known is not complete

“Well characterised” safety still leaves rare harms to be found. Semaglutide was authorised in the EU in 2018 after large trials, and in June 2025 the EMA’s safety committee concluded that NAION, an eye condition that can cause sudden loss of vision, is a very rare side effect: one that may affect up to 1 in 10,000 people taking it.15,11 Trials of a few thousand people can easily miss a harm that rare; wider use over years can find it.

This rubric is not GRADE

Guideline groups worldwide use GRADE to rate how much confidence a body of evidence deserves for one specific question, from “high” to “very low”. It starts randomised trials high and observational studies low, and moves them down for study limitations, inconsistency, indirectness, imprecision and reporting bias.16 Our rubric does something coarser and different: it describes the overall state of the evidence on a compound, across all its claimed uses. It does not tell anyone whether to use a treatment, and it cannot replace a GRADE assessment for a clinical question.

How a grade changes

Can a grade change?

Yes. If new evidence is published or we find a mistake, it changes. Every change is logged.
A grade changes only for a published reason, and every change is logged.
  1. New evidence is published, for example a trial reported in full, or an independent laboratory repeats a key experiment. Or a reader or editor finds an error.
  2. An editor checks it against the rules on this page.
  3. The data file is updated. The grade is stored once and shown in every language, so it cannot drift between translations.
  4. The reason is rewritten on the compound page, saying what changed and why.
  5. The change is logged with its date and the pages it affects.

Every change to a grade is listed in the corrections log, with its date. How we choose and check sources is set out in the editorial policy.

In detail: What would move a grade, with examples , about 1 minute to read

Grades move in both directions, and we would report either.

  • Human clinical evidence moves up when a trial is published in full. If the old BPC-157 phase 2 trial were published with its full data, it would count; so would the results of a registered trial, once published.3 It never moves up for a press release or a registration.
  • Independence moves up when other laboratories repeat the key findings, and stays where it is when new papers only review old ones. Between 2024 and 2026, most new BPC-157 records in PubMed (34 of 52) did not list the Zagreb group’s leader as an author, but more than half of those were tagged as reviews, comments, letters or editorials, which do not count as repeats.1
  • Safety moves from “uncharacterised” to “partial” only with systematic safety data from people, collected in a study, not with an absence of reports.
  • Any grade moves down if we find we counted wrongly, or if a published study is retracted.

The Croatian lab sets out the five things that would change the BPC-157 picture.

Sources

Every claim on this page links to one of these sources. Scholarly sources link to their DOI; regulatory sources to the regulator's own page.

In detail: All 16 sources, numbered as in the text , about 3 minutes to read
  1. National Library of Medicine (2026). PubMed search, 20 October 2026: ("BPC 157"[tiab] OR "BPC-157"[tiab] OR "BPC157"[tiab] OR "PL 14736"[tiab] OR "PL-14736"[tiab] OR "bepecin"[tiab] OR "BPC 157"[nm]) — 235 records, 175 with Sikiric P as author. PubMed. Dataset pubmed.ncbi.nlm.nih.gov (opens an external site) — accessed 20 October 2026 ↩
  2. Poolton JT, Minett J, Kazmi A (2026). Human evidence for BPC-157 in orthopaedic and regenerative medicine: a systematic review of efficacy and safety. Acta Orthopaedica Belgica 92. Review doi:10.52628/92.3.15837 (opens an external site) ↩
  3. U.S. Food and Drug Administration (2026). FDA Briefing Document for BPC-157-Related Bulk Drug Substances (BPC-157 (free base) and BPC-157 acetate), Pharmacy Compounding Advisory Committee meeting, 23–24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
  4. Begley CG, Ellis LM (2012). Drug development: Raise standards for preclinical cancer research. Nature 483:531-533. Research article doi:10.1038/483531a (opens an external site) ↩
  5. Errington TM, Mathur M, Soderberg CK, Denis A, Perfito N, Iorns E, Nosek BA (2021). Investigating the replicability of preclinical cancer biology. eLife 10:e71601. Research article doi:10.7554/eLife.71601 (opens an external site) ↩
  6. National Library of Medicine (2026). PubMed searches, 20 October 2026: (retatrutide[tiab] OR LY3437943[tiab]) — 207 records; AND randomized controlled trial[pt] — 10 records, 0 after NOT lilly[ad]. PubMed. Dataset pubmed.ncbi.nlm.nih.gov (opens an external site) — accessed 20 October 2026 ↩
  7. Hathaway JT, Shah MP, Hathaway DB, Zekavat SM, Krasniqi D, Gittinger JW, et al. (2024). Risk of nonarteritic anterior ischemic optic neuropathy in patients prescribed semaglutide. JAMA Ophthalmology 142:732-739. Research article doi:10.1001/jamaophthalmol.2024.2296 (opens an external site) ↩
  8. Pasternak B, Wintzell V, Hviid A, Eliasson B, Gudbjörnsdottir S, Jonasson C, et al. (2024). Glucagon-like peptide 1 receptor agonist use and risk of thyroid cancer: Scandinavian cohort study. BMJ 385:e078225. Research article doi:10.1136/bmj-2023-078225 (opens an external site) ↩
  9. European Medicines Agency (2024). Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 8-11 April 2024. Regulator ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  10. Macleod MR, Lawson McLean A, Kyriakopoulou A, Serghiou S, et al. (2015). Risk of Bias in Reports of In Vivo Research: A Focus for Improvement. PLoS Biology 13:e1002273. Research article doi:10.1371/journal.pbio.1002273 (opens an external site) ↩
  11. European Medicines Agency (2025). PRAC concludes eye condition NAION is a very rare side effect of semaglutide medicines Ozempic, Rybelsus and Wegovy. Regulator ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  12. Ashraf AR, Mackey TK, Vida RG, Kulcsár G, Schmidt J, Balázs O, Domián BM, Li J, Csákó I, Fittler A (2024). Multifactor Quality and Safety Analysis of Semaglutide Products Sold by Online Sellers Without a Prescription: Market Surveillance, Content Analysis, and Product Purchase Evaluation Study. Journal of Medical Internet Research 26:e65440. Research article doi:10.2196/65440 (opens an external site) ↩
  13. U.S. Food and Drug Administration (2026). FDA Briefing Document for TB-500-Related Bulk Drug Substances (TB-500 (free base) and TB-500 acetate), Pharmacy Compounding Advisory Committee meeting, 23–24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
  14. Sena ES, van der Worp HB, Bath PM, Howells DW, Macleod MR (2010). Publication bias in reports of animal stroke studies leads to major overstatement of efficacy. PLoS Biology 8:e1000344. Research article doi:10.1371/journal.pbio.1000344 (opens an external site) ↩
  15. European Medicines Agency (2026). Ozempic (semaglutide): EPAR — overview and product information. Official product information ema.europa.eu (opens an external site) — accessed 20 October 2026 ↩
  16. Guyatt GH, Oxman AD, Vist GE, Kunz R, Falck-Ytter Y, Alonso-Coello P, Schünemann HJ, et al. (2008). GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ 336:924-926. Research article doi:10.1136/bmj.39489.470347.AD (opens an external site) ↩