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In addition to these observed effects, mild to moderate responses such as gastrointestinal disturbance, cephalic discomfort, and localized dermal reactions at the administration site have also been reported in research subjects

The study investigated the relationship between protein concentration and the accuracy of the current method

To rule out inferiority, the FDA required CVOTs to show an upper boundary risk ratio of 1.3 (post approval), utilizing a two-sided 95% confidence interval (CI), for major adverse cardiovascular events (MACE) [55]

Liraglutide The injectable GLP-1 analogue, liraglutide (Victoza), is FDA approved for once-daily subcutaneous administration in combination with diet and exercise for the treatment of patients with T2DM