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Consistency matters Results depend on ongoing use

FDA's evaluation concluded that the criteria weighed against placement on the list, citing inadequate physicochemical characterization, immunogenicity concerns from impurities and aggregates, lack of clinical effectiveness data for any approved use, and absence of published human exposure data for the proposed subcutaneous and topical routes

doi:10.3390/ijms24021703 Contributor A

Altered PER1 expression has been linked to changes in tumor behavior and sensitivity to external stressors

They may recommend lowering the dosage or switching to a different GLP-1 medication

NAD+ injections are not FDA-approved