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Moving peptides from category 2 to category 1 means: Compounding pharmacies will again be able to formulate these peptides for patient use Physicians will be able to prescribe them as part of supervised treatment plans Research institutions will have greater ability to conduct clinical studies on these compounds FDA-inspected facilities will handle manufacturing, reducing reliance on unregulated sources What it does not mean is that these peptides will be available over the counter

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Epigenetically mediated pathogenic effects of phenanthrene on regulatory T cells