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Message: <blockquote data-quote="tareload" data-source="post: 244600">Previous comments I made on this (my oncology buddy shot me right down, see above):Additional reading and review I've done indicates the prion issue is more theoretical than the fact that urinary-derived hCG has a whole host of growth factors/cytokines the concentrations of which are highly variable and depend on manufacturer and batch.  I've attached a few pertinent publications for your review if interested (perhaps you have already read them).  Interesting that urinary-derived hCG now being trial for immunosuppression with various ailments (see second attachment).  This researcher has spent a bit of effort summarizing his findings:  xttp://hcglab.com/hcg-the-root-of-human-evolution/using-hcg-as-a-dietary-aid-or-as-a-anabolic-steroid-promoter/ He's recently written a book on it: <a href="https://www.elsevier.com/books/human-chorionic-gonadotropin-hcg/cole/978-0-12-800749-5" target="_blank">Human Chorionic Gonadotropin (hCG) - 2nd Edition</a> My reading of relevant literature is there is a lot of correlation/causation in the literature wrt to hyperglycosylated hCG and beta-core fragment and its effects on the body. Clearly, there is a lot of other growth factors/cytokines in the u-hCG but I don't see the FDA getting too worried about it after being on the market for 50 years?? Maybe they should.  Checking the FDA orange book I see u-hCG was last approved in 1982.  A lot has been learned since then regarding various forms and degradation products of hCG. I realize risk vs reward for any medication. From Yarram 2004: From link I attached above: Based on this, you are in catch 22 whether you use rhCG or uhCG.Note you will see the website linked  above is now long done.[URL unfurl="true"]https://pubmed.ncbi.nlm.nih.gov/15237021/[/URL][URL unfurl="true"]https://pubmed.ncbi.nlm.nih.gov/26389834/[/URL]</blockquote>

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