re how B impacts the gut am assuming largely in a compensatory (+) way given the apparent major Defensin/Mucin deficiency in IBD, esp Crohn's ---- the academic research compiled by IPIX is rather compelling as to its potential.
"Defensin Therapeutics", per below, sounds almost as good as the "Brilacidin Platform" --- except we have a drug in multiple mid-stage trials, reality not concept.
How do you get the antiinflammatory benefit without killing off gut bacteria since B also has major antibacterial action?
I’m not informed enough to know exactly where in the GI tract Brilacidin would be introduced (excreted) but the drug apparently is not metabolized and I don’t remember seeing any GI issues with the ABSSI trial. “The majority of brilacidin (PMX-30063) was eliminated unchanged via fecal route and there was no indication of metabolism in liver or kidney.”