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FDA isnt going to do shit without proper human studies and no pharma fag company thinks they can make money off it, fuck pharma and fuck the FDA and the epstein class If this happens, demand for research-grade BPC-157 is likely to spike
Particularly, adults over 50, vegans and vegetarians, people with digestive conditions, and anyone whos had stomach surgery may all be at an increased risk for low B12 levels
And so again, Marty talks about this in his book, so I know he's aligned with a lot of these viewpoints
Pharmacokinetic parameters after intravenous administration in rats showed Dihexa possessed a long half-life of 12.68 days and was extensively distributed, indicated by a large volume of distribution (Va)
This endogenous, potent mechanism is the pharmacological underpinning of the microdosing hypothesis for BPC-157
Tirzepatide is an FDA-approved drug with completed Phase 3 obesity trials, while cagrilintide is investigational, with monotherapy data only through Phase 2 and its strongest results coming from the CagriSema combination
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