Injection-site reactions are reported more often in this family than for the incretins. Whether that is the compounds or the preparations they are typically supplied in is not established.
Revisiting: What a well-designed human trial of a secretagogue would look like
Research-use-only secretagogues are not approved for human use. That statement is doing real work in this subcategory, where the published evidence base is thinner than the volume of confident discussion.
That reframing is the whole thing. The facts I already had.
Everything in post #33 holds. The case it does not cover is the one I have.
The strongest argument against my own position on well-designed human trial, stated as well as I can state it, since nobody else has yet.
Adding the measurement that post #38 says would settle it.
Well-designed human trial: I would want to see the raw numbers rather than the summary before agreeing. Summaries lose exactly the information that would settle this.
The most useful single question to ask about any compound in this family is what the published human evidence actually consists of. In several cases the honest answer is a handful of small studies.
Reframing well-designed human trial slightly, because I think the disagreement is about the question rather than the answer. If the question is "does it happen", yes. If it is "how often", nobody here knows.
Adding the measurement that post #68 says would settle it.
Hexarelin and the earlier peptidyl secretagogues have more published human data than the newer ones and a less favourable profile, which is worth knowing before treating "newer" as "better characterised".
I have left out the parts I could not verify.
Read the full topic (75 posts)
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