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Compounds · Repair & healing peptides · continued

Reading a preclinical wound-healing model and its relevance to a human tendon — a second dataset posts 61–70

This is a continuation of a long topic, addressed by post number rather than by page. Start at post 1.

CN
c.niemelTL3Regular14 Mar 2026#61

I think the Reading a preclinical wound-healing model question is answerable and has not been answered, which is a more optimistic position than most of this thread.

24 likes 4mo
RM
r.mwangiTL214 Mar 2026#62

Reading a preclinical wound-healing model would be much easier to settle if anyone reported the denominator. Almost nobody reports the denominator.

11 likes 4mo
EC
excursion_checkTL3Regular14 Mar 2026#63
j.marchetti, post #7: Post #3 and I disagree about the size of the effect, not about the direction. For anyone arriving from search engines: this subcategory discusses published preclinical work and the absence of published clinical work. It does not endorse or recommend these compounds. Go to post

Worth separating two things that post #59 runs together.

The absence of adequately powered published randomised human trials is the central fact about BPC-157. This site states that plainly rather than hedging. Mechanistic plausibility does not substitute for it.

A modest claim, modestly supported.

1 like in reply to #7 4mo
SV
s.vanheckeTL214 Mar 2026#64
TT
taper_tableTL3Regular14 Mar 2026 · edited#65

Distinguishing three things in the Reading a preclinical wound-healing model discussion that keep getting used interchangeably: the observation, the proposed mechanism, and the recommendation that gets attached to both.

17 likes 4mo
PB
p.boatengTL214 Mar 2026#66

The absence of human trials means there is no established dose, no established interval and no established duration. Protocols circulating in this space are convention rather than evidence and should be described as such.

If that reads as pedantic, it is, and it has saved me twice.

7 likes 4mo
LC
l.chevalierTL3Regular14 Mar 2026#67
p.boateng, post #66: The absence of human trials means there is no established dose, no established interval and no established duration. Protocols circulating in this space are convention rather than evidence and should be described as such. If that reads as pedantic, it is, and it has saved me twice. Go to post

On post #63 — agreed on the reasoning, with one qualification.

For anyone arriving from search engines: this subcategory discusses published preclinical work and the absence of published clinical work. It does not endorse or recommend these compounds.

0 likes in reply to #66 4mo
MA
m.adebayoTL215 Mar 2026#68

Right — I had this wrong and I am glad to have read it before it mattered.

0 likes 4mo
SD
s.dziedzicTL215 Mar 2026#69

Where I part company with post #67, and it is a narrow parting.

BPC-157's published evidence is overwhelmingly preclinical and mostly rodent. That is not a dismissal — it is the state of the literature, and any discussion that starts elsewhere is starting from something that is not there.

0 likes 4mo
CA
c.adebayoTL215 Mar 2026#70
r.restrepo, post #38: Answering the question post #36 raises rather than the one it answers. BPC-157's published evidence is overwhelmingly preclinical and mostly rodent. That is not a dismissal — it is the state of the literature, and any discussion that starts elsewhere is starting from something that is not there. Go to post

Post #67 is the version of this I will quote in future. One addition.

Research use only, not approved for human use, and in this family that statement carries more weight than usual because the published human safety data is effectively absent rather than merely limited.

That has been true for the cases I have seen and I have not seen many.

23 likes in reply to #38 4mo

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