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Food & Drug Administration’s 503a bulks list, indicating steep restrictions owing to significant safety risks.15 With many such drugs, a person is denied access unless they qualify for an exemption, which would require that a licensed clinician has deemed the treatment to be “necessary for the identified patient.”16 With dihexa, the obstacle then is proving that it would be a more medically necessary option than some other treatment, when it pales in terms of efficacy and safety research even when compared with other category 2 cognitive health peptides

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This precision medicine approach potentially enables clinicians to individualize treatment regimens through the selection of the best strain, dose, and combination therapies to maximize efficacy and minimize toxicity