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As a research peptide, AOD-9604 is not manufactured under the same regulatory oversight as pharmaceutical products

Disability worsening lasting three months or more was observed in 10.9% of patients on Kesimpta compared with 15% of those on Aubagio a 34% risk reduction while the rates of disability worsening lasting at least six months were 8.1% for Kesimpta and 12% for Aubagio, a 32% reduction

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Proper clinical practice protocols ensure patient safety through appropriate screening for contraindications and monitoring for potential adverse effects

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