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Data analysis We explored the transitivity assumption by comparing the distribution of potential effect modifiers (baseline HbA 1c and body weight) across treatment comparisons [14]

Lack of Safety Data for Different Administration Routes FDA regulations require independent toxicological assessments for different administration routes, including topical, injectable, and oral administration

Following injection, maximal plasma concentrations are reached within approximately 1 hour

Thereafter, all cells were collected for quantitative analysis by flow cytometry (Invitrogen, Attune NxT, USA) and FlowJo 7.6.1

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