Topic desk · 3 reviewed briefs
Recovery and repair claims
Track the leap from cells and animals to claims about tendon, muscle, wound, and post-injury recovery in people.
Evidence boundary
Biological plausibility is not a clinical repair outcome. Fragment identity, route, sterility, and impurity risks remain part of the evidence.
- Reviewed briefs
- 3
- Established contexts
- 0
- Reviewed claims
- 9
Before accepting a claim
Ask the question the promotion leaves out.
- 01
Is the finding from cells, animals, human pharmacology, or a controlled outcome trial?
- 02
Is the marketed molecule identical to the one in the source?
- 03
Does the claim ignore product-quality and anti-doping boundaries?
Connected briefs
Compare evidence without flattening it.
BPC-157
An investigational peptide with a sizable preclinical literature, early human work, and a large gap between biological signal and proven clinical effect.
3 reviewed claims · Open brief ↗TB-500
A seven-amino-acid thymosin fragment promoted for repair despite an unresolved human-outcome gap, significant product questions, and anti-doping prohibition.
3 reviewed claims · Open brief ↗GHK-Cu
A copper-binding tripeptide with topical and laboratory research that does not validate injectable, whole-body, or longevity claims.
3 reviewed claims · Open brief ↗