Evidence: how to judge a health claim
In short
Reading the whole page takes about 2 minutes.
- A claim is only as good as the study behind it. These pages show you how to check.
- A result in rats or cells is a first step. It does not show what works in people.
- We grade evidence on four separate questions. We never add them into one score.
- Who paid for a study matters. It does not make a result false, but it calls for checks.
Why read about evidence?
| Your question | Read |
|---|---|
| What kind of study is this, and what can it show? | How to read a study |
| It worked in rats. Will it work in people? | The translation gap |
| How strong is the evidence for this compound? | Evidence grading |
| Who paid, and does that matter? | Conflicts of interest |
Many peptides sold outside pharmacies, such as BPC-157, TB-500 and KPV, have been studied almost only in cells and animals. Some have hardly been studied at all.1,2,3 Animal studies are a real start. But in one large review, only 5 in 100 treatments tested in animals were later approved for use in people.4
Who paid matters too. Studies paid for by a company more often report good results for its product.5 That does not make them wrong. It means someone independent should check.
These pages give no doses and no advice on what to use. They help you judge what you read. If you already use a product, see product risk and the warning signs.
The evidence pages
Where should I start?
- How to read a study
From cell dishes to large trials: what each kind of study can answer, and the questions to ask of any abstract or headline before you trust it.
- The translation gap
Why results in rats and mice so often fail in people: species differences, lab-made injuries, small biased studies, and why animal doses do not scale.
- Evidence grading
The rubric behind every evidence profile on this site: four separate axes, the thresholds for each, the claim badges, their limits and how a grade changes.
- Conflicts of interest
How to spot a sponsored study, a seller's review, a paid expert or influencer, ghost-writing and predatory journals, and how much checking a conflict calls for.
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.
- (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 ↩
- (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 ↩
- (2026). FDA Briefing Document for KPV-Related Bulk Drug Substances (KPV (free base) and KPV acetate), Pharmacy Compounding Advisory Committee meeting, 23-24 July 2026. Regulator fda.gov (opens an external site) — accessed 20 October 2026 ↩
- (2024). Analysis of animal-to-human translation shows that only 5% of animal-tested therapeutic interventions obtain regulatory approval for human applications. PLoS Biology 22:e3002667. Research article doi:10.1371/journal.pbio.3002667 (opens an external site) ↩
- (2017). Industry sponsorship and research outcome. Cochrane Database of Systematic Reviews 2:MR000033. Review doi:10.1002/14651858.MR000033.pub3 (opens an external site) ↩